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dbVar

Database of genomic structural variation

nsv5645900

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Ebert 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: 218 SVs from 25 studies. See in: genome view

Submitted genomic77,566,461-77,566,461

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5645900	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000013.11	Chr13	77,566,461	77,566,461
nsv5645900	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000013.10	Chr13	78,140,596	78,140,596

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17098334	insertion	SAMN00000485	Sequencing	Sequence alignment	1,404

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17098334	Submitted genomic		NC_000013.11:g.775 66461_77566462ins1 920	GRCh38 (hg38)		NC_000013.11	Chr13	77,566,461	77,566,461
nssv17098334	Remapped	Perfect	NC_000013.10:g.781 40596_78140597ins1 920	GRCh37.p13	First Pass	NC_000013.10	Chr13	78,140,596	78,140,596

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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