A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1154298



Internal ID15873655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35366022..35441182hg38UCSC Ensembl
Innerchr6:35333799..35408959hg19UCSC Ensembl
Innerchr6:35441777..35516937hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3875161
hg1975161
hg1875161
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602908
Supporting Variants
SamplesHGDP00286
Known GenesPPARD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1154298
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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