A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv777140



Internal ID15724410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:62771357..62787614hg38UCSC Ensembl
Innerchr11:62538829..62555086hg19UCSC Ensembl
Innerchr11:62295405..62311662hg18UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3816258
hg1916258
hg1816258
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555175
Supporting Variants
Samples
Known GenesTAF6L, TMEM179B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv777140
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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