A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601339



Internal ID16042062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29893503..29943266hg38UCSC Ensembl
Innerchr6:29861280..29911043hg19UCSC Ensembl
Innerchr6:29969259..30019022hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3849764
hg1949764
hg1849764
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10347n54
Supporting Variantsnssv1051985, nssv1051986
Samples
Known GenesHCG4B, HLA-A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601339
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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