A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601874



Internal ID16389283
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 StatusM
Merged Variantsdgv10453n54
Supporting Variantsnssv1053380, nssv1154257, nssv1053379, nssv1053376, nssv1154258, nssv1053378, nssv1053374, nssv1154256, nssv1053375, nssv1053377
SamplesHGDP00945, HGDP00771, HGDP01251
Known GenesHCG26, HCP5, MICA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601874
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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