A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601904



Internal ID16042627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31392612..31491965hg38UCSC Ensembl
Innerchr6:31360389..31459742hg19UCSC Ensembl
Innerchr6:31468368..31567721hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3899354
hg1999354
hg1899354
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10453n54
Supporting Variantsnssv1154282, nssv1053479, nssv1053477, nssv1053478, nssv1053476
SamplesHGDP00739
Known GenesHCG26, HCP5, MICA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601904
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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