A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658504



Internal ID15395156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:191347603..191350499hg38UCSC Ensembl
Innerchr3:191065392..191068288hg19UCSC Ensembl
Innerchr3:192548086..192550982hg18UCSC Ensembl
Innerchr3:192548094..192550990hg17UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg382897
hg192897
hg182897
hg172897
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516440
Supporting Variants
Samples
Known GenesCCDC50
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv658504
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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