A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3511461



Internal ID18809742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:127177506..127191913hg38UCSC Ensembl
Innerchr11:127047401..127061808hg19UCSC Ensembl
Innerchr11:126552611..126567018hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3814408
hg1914408
hg1814408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044960
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3511461
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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