A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1051882



Internal ID15558382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29891740..29913467hg38UCSC Ensembl
Innerchr6:29859517..29881244hg19UCSC Ensembl
Innerchr6:29967496..29989223hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3821728
hg1921728
hg1821728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601312
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)nssv1051882
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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