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dbVar

Database of genomic structural variation

nsv5601343

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:84

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

Submitted genomic137,263,295-137,263,378

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5601343	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	137,263,295	137,263,378
nsv5601343	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	140,157,747	140,157,830

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17161099	deletion	HG03371	Sequencing	Sequence alignment	2,852

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17161099	Submitted genomic		NC_000009.12:g.137 263295_137263378de lA	GRCh38 (hg38)		NC_000009.12	Chr9	137,263,295	137,263,378
nssv17161099	Remapped	Perfect	NC_000009.11:g.140 157747_140157830de lA	GRCh37.p13	First Pass	NC_000009.11	Chr9	140,157,747	140,157,830

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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