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dbVar

Database of genomic structural variation

nsv6289789

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: 78 SVs from 20 studies. See in: genome view

Submitted genomic9,816,882-9,816,882

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6289789	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	9,816,882	9,816,882
nsv6289789	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	9,720,199	9,720,199

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17938471	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17938471	Submitted genomic		NC_000017.11:g.981 6882_9816883ins54	GRCh38 (hg38)		NC_000017.11	Chr17	9,816,882	9,816,882
nssv17938471	Remapped	Perfect	NC_000017.10:g.972 0199_9720200ins54	GRCh37.p13	First Pass	NC_000017.10	Chr17	9,720,199	9,720,199

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)
nssv17938471	<0.001	1	2108

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