A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv778565



Internal ID15725835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67143355..67148921hg38UCSC Ensembl
Innerchr11:66910826..66916392hg19UCSC Ensembl
Innerchr11:66667402..66672968hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg385567
hg195567
hg185567
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555252
Supporting Variants
Samples
Known GenesKDM2A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv778565
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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