A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601873



Internal ID16042596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31387541..31481550hg38UCSC Ensembl
Innerchr6:31355318..31449327hg19UCSC Ensembl
Innerchr6:31463297..31557306hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3894010
hg1994010
hg1894010
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10453n54
Supporting Variantsnssv1053372, nssv1154254, nssv1053371, nssv1053373, nssv1154255
SamplesHGDP00753, HGDP00852
Known GenesHCG26, HCP5, MICA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601873
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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