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dbVar

Database of genomic structural variation

nsv5977925

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Almarri et al. 2020

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: 203 SVs from 36 studies. See in: genome view

Submitted genomic32,348,302-32,348,302

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5977925	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000013.11	Chr13	32,348,302	32,348,302
nsv5977925	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000013.10	Chr13	32,922,439	32,922,439

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17380059	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17380059	Submitted genomic		NC_000013.11:g.323 48302_32348303ins1 92	GRCh38 (hg38)		NC_000013.11	Chr13	32,348,302	32,348,302
nssv17380059	Remapped	Perfect	NC_000013.10:g.329 22439_32922440ins1 92	GRCh37.p13	First Pass	NC_000013.10	Chr13	32,922,439	32,922,439

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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