A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701558



Internal ID15091524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:133428712..133436250hg38UCSC Ensembl
Innerchr11:133298607..133306145hg19UCSC Ensembl
Innerchr11:132803817..132811355hg18UCSC Ensembl
Innerchr11:132803817..132811355hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg387539
hg197539
hg187539
hg177539
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525431
Supporting Variants
Samples
Known GenesOPCML
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701558
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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