A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528351



Internal ID15108958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35410145..35498009hg38UCSC Ensembl
Innerchr6:35377922..35465786hg19UCSC Ensembl
Innerchr6:35485900..35573764hg18UCSC Ensembl
Innerchr6:35485900..35573764hg17UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3887865
hg1987865
hg1887865
hg1787865
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704935
Samples
Known GenesFANCE, MIR7111, PPARD, RPL10A, TEAD3, TULP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528351
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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