A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601267



Internal ID16388676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29886178..29907748hg38UCSC Ensembl
Innerchr6:29853955..29875525hg19UCSC Ensembl
Innerchr6:29961934..29983504hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3821571
hg1921571
hg1821571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10345n54
Supporting Variantsnssv1051805, nssv1051806, nssv1051807
Samples
Known GenesHLA-H
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601267
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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