A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703752



Internal ID15093718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:295343..620599hg38UCSC Ensembl
Innerchr11:295343..620599hg19UCSC Ensembl
Innerchr11:285343..610599hg18UCSC Ensembl
Innerchr11:285343..610599hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38325257
hg19325257
hg18325257
hg17325257
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527327
Supporting Variants
Samples
Known GenesANO9, ATHL1, B4GALNT4, C11orf35, CDHR5, HRAS, IFITM1, IFITM2, IFITM3, IFITM5, IRF7, LOC143666, LRRC56, MIR210, MIR210HG, PHRF1, PKP3, PTDSS2, RASSF7, RNH1, SIGIRR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703752
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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