A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601475



Internal ID16042198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29995402..30010196hg38UCSC Ensembl
Innerchr6:29963179..29977973hg19UCSC Ensembl
Innerchr6:30071158..30085952hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3814795
hg1914795
hg1814795
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1052256
Samples
Known GenesHLA-J, ZNRD1-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601475
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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