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dbVar

Database of genomic structural variation

nsv5900327

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:784

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: 162 SVs from 33 studies. See in: genome view

Submitted genomic132,962,337-132,963,120

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5900327	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	132,962,337	132,963,120
nsv5900327	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	133,719,910	133,720,693

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17404353	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17404353	Submitted genomic		NC_000002.12:g.132 962337_132963120de l	GRCh38 (hg38)		NC_000002.12	Chr2	132,962,337	132,963,120
nssv17404353	Remapped	Perfect	NC_000002.11:g.133 719910_133720693de l	GRCh37.p13	First Pass	NC_000002.11	Chr2	133,719,910	133,720,693

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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