A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153632



Internal ID15879064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:13426307..13519202hg38UCSC Ensembl
Innerchr6:13426539..13519434hg19UCSC Ensembl
Innerchr6:13534518..13627413hg18UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3892896
hg1992896
hg1892896
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600994
Supporting Variants
SamplesHGDP01302
Known GenesGFOD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153632
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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