A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699125



Internal ID15435777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:154599740..154718407hg38UCSC Ensembl
Innerchr3:154317529..154436196hg19UCSC Ensembl
Innerchr3:155800223..155918890hg18UCSC Ensembl
Innerchr3:155800231..155918898hg17UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38118668
hg19118668
hg18118668
hg17118668
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523376
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699125
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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