A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601901



Internal ID16042624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31392612..31483699hg38UCSC Ensembl
Innerchr6:31360389..31451476hg19UCSC Ensembl
Innerchr6:31468368..31559455hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3891088
hg1991088
hg1891088
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10453n54
Supporting Variantsnssv1154275, nssv1053462, nssv1053465, nssv1154276, nssv1053441, nssv1053449, nssv1053446, nssv1053444, nssv1053447, nssv1053457, nssv1053455, nssv1053466, nssv1053456, nssv1154277, nssv1154279, nssv1053453, nssv1053454, nssv1053464, nssv1053458, nssv1053445, nssv1053443, nssv1053463, nssv1053440, nssv1053461, nssv1053459, nssv1053442, nssv1053450, nssv1154280, nssv1053460, nssv1053468, nssv1053452, nssv1053448, nssv1154278, nssv1053451, nssv1053467, nssv1154274
SamplesHGDP00699, HGDP00878, HGDP00675, HGDP01096, HGDP00920, HGDP01240, HGDP00876
Known GenesHCG26, HCP5, MICA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601901
Frequency
Sample Size17421
Observed Gain0
Observed Loss36
Observed Complex0
Frequencyn/a


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