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dbVar

Database of genomic structural variation

nsv5580162

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:66

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: 827 SVs from 78 studies. See in: genome view

Submitted genomic168,075,852-168,075,917

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5580162	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	168,075,852	168,075,917
nsv5580162	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	168,476,532	168,476,597

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17148815	deletion	SAMN00006579	Sequencing	Sequence alignment	23,265

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17148815	Submitted genomic		NC_000006.12:g.168 075852_168075917de lC	GRCh38 (hg38)		NC_000006.12	Chr6	168,075,852	168,075,917
nssv17148815	Remapped	Perfect	NC_000006.11:g.168 476532_168476597de lC	GRCh37.p13	First Pass	NC_000006.11	Chr6	168,476,532	168,476,597

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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