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dbVar

Database of genomic structural variation

nsv5624716

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: 118 SVs from 31 studies. See in: genome view

Submitted genomic150,167,973-150,167,973

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5624716	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	150,167,973	150,167,973
nsv5624716	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	150,489,109	150,489,109

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17158038	insertion	SAMN00006579	Sequencing	Sequence alignment	23,265

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17158038	Submitted genomic		NC_000006.12:g.150 167973_150167974in s1076	GRCh38 (hg38)		NC_000006.12	Chr6	150,167,973	150,167,973
nssv17158038	Remapped	Perfect	NC_000006.11:g.150 489109_150489110in s1076	GRCh37.p13	First Pass	NC_000006.11	Chr6	150,489,109	150,489,109

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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