A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601252



Internal ID16388661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29883666..29927334hg38UCSC Ensembl
Innerchr6:29851443..29895111hg19UCSC Ensembl
Innerchr6:29959422..30003090hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3843669
hg1943669
hg1843669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10344n54
Supporting Variantsnssv1051755, nssv1051761, nssv1051759, nssv1051753, nssv1051756, nssv1051757, nssv1051758, nssv1051754, nssv1051760, nssv1051752, nssv1051763, nssv1051762
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)nsv601252
Frequency
Sample Size17421
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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