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dbVar

Database of genomic structural variation

nsv6289754

Organism: Homo sapiens

Study:nstd214 (Naslavsky et al. 2022)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Naslavsky et al. 2022

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: 94 SVs from 21 studies. See in: genome view

Submitted genomic71,757,554-71,757,554

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6289754	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	71,757,554	71,757,554
nsv6289754	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	72,049,893	72,049,893

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17933174	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17933174	Submitted genomic		NC_000015.10:g.717 57554_71757555ins6 4	GRCh38 (hg38)		NC_000015.10	Chr15	71,757,554	71,757,554
nssv17933174	Remapped	Perfect	NC_000015.9:g.7204 9893_72049894ins64	GRCh37.p13	First Pass	NC_000015.9	Chr15	72,049,893	72,049,893

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv17933174	0.005	12	2322

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