A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694786



Internal ID15084752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:37940970..37982062hg38UCSC Ensembl
Innerchr3:37982461..38023553hg19UCSC Ensembl
Innerchr3:37957465..37998557hg18UCSC Ensembl
Innerchr3:37957465..37998557hg17UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3841093
hg1941093
hg1841093
hg1741093
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522017
Supporting Variants
Samples
Known GenesCTDSPL, MIR26A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694786
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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