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dbVar

Database of genomic structural variation

nsv5662710

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: 209 SVs from 42 studies. See in: genome view

Submitted genomic82,586,259-82,586,259

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5662710	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	82,586,259	82,586,259
nsv5662710	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	80,544,135	80,544,135

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17098386	insertion	SAMN00006466	Sequencing	Sequence alignment	4,625

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17098386	Submitted genomic		NC_000017.11:g.825 86259_82586260ins6 435	GRCh38 (hg38)		NC_000017.11	Chr17	82,586,259	82,586,259
nssv17098386	Remapped	Perfect	NC_000017.10:g.805 44135_80544136ins6 435	GRCh37.p13	First Pass	NC_000017.10	Chr17	80,544,135	80,544,135

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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