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dbVar

Database of genomic structural variation

nsv5660949

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: 311 SVs from 47 studies. See in: genome view

Submitted genomic530,503-530,503

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5660949	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	530,503	530,503
nsv5660949	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	530,503	530,503

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17074809	insertion	SAMN00006581	Sequencing	Sequence alignment	289

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17074809	Submitted genomic		NC_000011.10:g.530 503_530504ins57	GRCh38 (hg38)		NC_000011.10	Chr11	530,503	530,503
nssv17074809	Remapped	Perfect	NC_000011.9:g.5305 03_530504ins57	GRCh37.p13	First Pass	NC_000011.9	Chr11	530,503	530,503

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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