A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv778617



Internal ID16072573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:68039236..68050067hg38UCSC Ensembl
Innerchr11:67806703..67817534hg19UCSC Ensembl
Innerchr11:67563279..67574110hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3810832
hg1910832
hg1810832
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555284
Supporting Variants
Samples
Known GenesMIR6753, TCIRG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv778617
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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