A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1154258



Internal ID15530485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31387541..31483132hg38UCSC Ensembl
Innerchr6:31355318..31450909hg19UCSC Ensembl
Innerchr6:31463297..31558888hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3895592
hg1995592
hg1895592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601874
Supporting Variants
SamplesHGDP00945
Known GenesHCG26, HCP5, MICA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1154258
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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