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dbVar

Database of genomic structural variation

nsv5618417

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: 163 SVs from 26 studies. See in: genome view

Submitted genomic17,757,727-17,757,727

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5618417	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	17,757,727	17,757,727
nsv5618417	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	17,759,350	17,759,350

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17131942	insertion	SAMN00001695	Sequencing	Sequence alignment	6,153

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17131942	Submitted genomic		NC_000004.12:g.177 57727_17757728ins3 26	GRCh38 (hg38)		NC_000004.12	Chr4	17,757,727	17,757,727
nssv17131942	Remapped	Perfect	NC_000004.11:g.177 59350_17759351ins3 26	GRCh37.p13	First Pass	NC_000004.11	Chr4	17,759,350	17,759,350

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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