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dbVar

Database of genomic structural variation

nsv5647514

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: 117 SVs from 29 studies. See in: genome view

Submitted genomic34,286,082-34,286,082

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5647514	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	34,286,082	34,286,082
nsv5647514	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	34,307,629	34,307,629

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17074017	insertion	SAMN00007824	Sequencing	Sequence alignment	1,699

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17074017	Submitted genomic		NC_000011.10:g.342 86082_34286083ins1 49	GRCh38 (hg38)		NC_000011.10	Chr11	34,286,082	34,286,082
nssv17074017	Remapped	Perfect	NC_000011.9:g.3430 7629_34307630ins14 9	GRCh37.p13	First Pass	NC_000011.9	Chr11	34,307,629	34,307,629

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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