A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1051879



Internal ID15558379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29891740..29908663hg38UCSC Ensembl
Innerchr6:29859517..29876440hg19UCSC Ensembl
Innerchr6:29967496..29984419hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3816924
hg1916924
hg1816924
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601311
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1051879
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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