A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601871



Internal ID16042594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31387042..31483699hg38UCSC Ensembl
Innerchr6:31354819..31451476hg19UCSC Ensembl
Innerchr6:31462798..31559455hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3896658
hg1996658
hg1896658
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10453n54
Supporting Variantsnssv1053370, nssv1053368, nssv1053366, nssv1053369, nssv1053367
Samples
Known GenesHCG26, HCP5, MICA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601871
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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