A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601254



Internal ID16388663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29883666..29928644hg38UCSC Ensembl
Innerchr6:29851443..29896421hg19UCSC Ensembl
Innerchr6:29959422..30004400hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3844979
hg1944979
hg1844979
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10344n54
Supporting Variantsnssv1051771, nssv1051770, nssv1051775, nssv1051777, nssv1051778, nssv1051766, nssv1051769, nssv1051767, nssv1051773, nssv1051776, nssv1051774, nssv1051768, nssv1051772
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)nsv601254
Frequency
Sample Size17421
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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