A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv777134



Internal ID15724404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:61486501..61570773hg38UCSC Ensembl
Innerchr11:61253973..61338245hg19UCSC Ensembl
Innerchr11:61010549..61094821hg18UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3884273
hg1984273
hg1884273
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555167
Supporting Variants
Samples
Known GenesLRRC10B, MIR4488, PPP1R32, SYT7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv777134
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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