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dbVar

Database of genomic structural variation

nsv5924206

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:50

Publication(s):Almarri et al. 2020

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: 187 SVs from 29 studies. See in: genome view

Submitted genomic165,813,313-165,813,362

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5924206	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	165,813,313	165,813,362
nsv5924206	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	166,226,801	166,226,850

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17410973	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17410973	Submitted genomic		NC_000006.12:g.165 813313_165813362de l	GRCh38 (hg38)		NC_000006.12	Chr6	165,813,313	165,813,362
nssv17410973	Remapped	Perfect	NC_000006.11:g.166 226801_166226850de l	GRCh37.p13	First Pass	NC_000006.11	Chr6	166,226,801	166,226,850

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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