A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174932



Internal ID15876077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:99617880..99631347hg38UCSC Ensembl
Innerchr11:99488611..99502078hg19UCSC Ensembl
Innerchr11:98993821..99007288hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3813468
hg1913468
hg1813468
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556086
Supporting Variants
SamplesHGDP00781
Known GenesCNTN5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174932
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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