A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601251



Internal ID16041974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29883666..29925263hg38UCSC Ensembl
Innerchr6:29851443..29893040hg19UCSC Ensembl
Innerchr6:29959422..30001019hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3841598
hg1941598
hg1841598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10344n54
Supporting Variantsnssv1051746, nssv1051750, nssv1051747, nssv1051745, nssv1051749, nssv1051744, nssv1051743, nssv1051751, nssv1051748
Samples
Known GenesHCG4B, HLA-H
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601251
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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