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dbVar

Database of genomic structural variation

nsv5589278

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:52

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: 467 SVs from 53 studies. See in: genome view

Submitted genomic137,436,391-137,436,442

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5589278	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	137,436,391	137,436,442
nsv5589278	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	140,330,843	140,330,894

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17160948	deletion	NA12329	Sequencing	Sequence alignment	1,517

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17160948	Submitted genomic		NC_000009.12:g.137 436391_137436442de lT	GRCh38 (hg38)		NC_000009.12	Chr9	137,436,391	137,436,442
nssv17160948	Remapped	Perfect	NC_000009.11:g.140 330843_140330894de lT	GRCh37.p13	First Pass	NC_000009.11	Chr9	140,330,843	140,330,894

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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