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dbVar

Database of genomic structural variation

nsv5656676

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: 100 SVs from 19 studies. See in: genome view

Submitted genomic111,628,416-111,628,416

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5656676	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	111,628,416	111,628,416
nsv5656676	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	111,499,140	111,499,140

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17072703	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
nssv17072703	Submitted genomic		NC_000011.10:g.111 628416_111628417in s61	GRCh38 (hg38)		NC_000011.10	Chr11	111,628,416	111,628,416
nssv17072703	Remapped	Perfect	NC_000011.9:g.1114 99140_111499141ins 61	GRCh37.p13	First Pass	NC_000011.9	Chr11	111,499,140	111,499,140

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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