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dbVar

Database of genomic structural variation

nsv5661765

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: 297 SVs from 27 studies. See in: genome view

Submitted genomic110,255,826-110,255,826

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5661765	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000013.11	Chr13	110,255,826	110,255,826
nsv5661765	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000013.10	Chr13	110,908,173	110,908,173

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17090211	insertion	SAMN00006579	Sequencing	Sequence alignment	23,265

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17090211	Submitted genomic		NC_000013.11:g.110 255826_110255827in s318	GRCh38 (hg38)		NC_000013.11	Chr13	110,255,826	110,255,826
nssv17090211	Remapped	Perfect	NC_000013.10:g.110 908173_110908174in s318	GRCh37.p13	First Pass	NC_000013.10	Chr13	110,908,173	110,908,173

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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