A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696816



Internal ID15086782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35411001..35569629hg38UCSC Ensembl
Innerchr6:35378778..35537406hg19UCSC Ensembl
Innerchr6:35486756..35645384hg18UCSC Ensembl
Innerchr6:35486756..35645384hg17UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38158629
hg19158629
hg18158629
hg17158629
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519370
Supporting Variants
Samples
Known GenesFANCE, MIR7111, PPARD, RPL10A, TEAD3, TULP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696816
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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