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dbVar

Database of genomic structural variation

nsv5906856

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:2,345

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: 218 SVs from 41 studies. See in: genome view

Submitted genomic131,602,463-131,604,807

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5906856	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	131,602,463	131,604,807
nsv5906856	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	132,360,036	132,362,380

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17399359	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17399359	Submitted genomic		NC_000002.12:g.131 602463_131604807de l	GRCh38 (hg38)		NC_000002.12	Chr2	131,602,463	131,604,807
nssv17399359	Remapped	Perfect	NC_000002.11:g.132 360036_132362380de l	GRCh37.p13	First Pass	NC_000002.11	Chr2	132,360,036	132,362,380

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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