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dbVar

Database of genomic structural variation

nsv4753585

Organism: Homo sapiens

Study:nstd199 (Quan et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Quan et al. 2021

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 446 SVs from 40 studies. See in: genome view

Remapped(Score: Perfect):46,160,996-46,160,996

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4753585	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000021.9	Chr21	46,160,996	46,160,996
nsv4753585	Remapped	Perfect	GRCh38.p12	ALT_REF_LOCI_1	Second Pass	NT_187626.1	Chr21\|NT_1 87626.1	20,059	20,059
nsv4753585	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000021.8	Chr21	47,580,910	47,580,910

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16273578	insertion	Sequencing	Split read mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16273578	Remapped	Perfect	NT_187626.1:g.2005 9_20060ins369	GRCh38.p12	Second Pass	NT_187626.1	Chr21\|NT_1 87626.1	20,059	20,059
nssv16273578	Remapped	Perfect	NC_000021.9:g.4616 0996_46160997ins36 9	GRCh38.p12	First Pass	NC_000021.9	Chr21	46,160,996	46,160,996
nssv16273578	Submitted genomic		NC_000021.8:g.4758 0910_47580911ins36 9	GRCh37 (hg19)		NC_000021.8	Chr21	47,580,910	47,580,910

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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