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dbVar

Database of genomic structural variation

nsv5977091

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

Submitted genomic32,243,426-32,243,426

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5977091	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	32,243,426	32,243,426
nsv5977091	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	30,570,445	30,570,445

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17377895	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17377895	Submitted genomic		NC_000017.11:g.322 43426_32243427ins6 8	GRCh38 (hg38)		NC_000017.11	Chr17	32,243,426	32,243,426
nssv17377895	Remapped	Perfect	NC_000017.10:g.305 70445_30570446ins6 8	GRCh37.p13	First Pass	NC_000017.10	Chr17	30,570,445	30,570,445

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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