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dbVar

Database of genomic structural variation

nsv5565650

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:171

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

Submitted genomic100,389,159-100,389,329

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5565650	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	100,389,159	100,389,329
nsv5565650	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	99,724,863	99,725,033

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17130586	deletion	HG03683	Sequencing	Sequence alignment	2,232

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17130586	Submitted genomic		NC_000005.10:g.100 389159_100389329de lG	GRCh38 (hg38)		NC_000005.10	Chr5	100,389,159	100,389,329
nssv17130586	Remapped	Perfect	NC_000005.9:g.9972 4863_99725033delG	GRCh37.p13	First Pass	NC_000005.9	Chr5	99,724,863	99,725,033

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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