A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601898



Internal ID16042621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31392612..31481550hg38UCSC Ensembl
Innerchr6:31360389..31449327hg19UCSC Ensembl
Innerchr6:31468368..31557306hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3888939
hg1988939
hg1888939
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10453n54
Supporting Variantsnssv1053426, nssv1053427, nssv1053425, nssv1154272
SamplesHGDP00110
Known GenesHCG26, HCP5, MICA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601898
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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