A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601256



Internal ID16388665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29883666..29933791hg38UCSC Ensembl
Innerchr6:29851443..29901568hg19UCSC Ensembl
Innerchr6:29959422..30009547hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3850126
hg1950126
hg1850126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10344n54
Supporting Variantsnssv1051784, nssv1051781, nssv1051780, nssv1051782, nssv1051783, nssv1051785, nssv1051786
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)nsv601256
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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