A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602949



Internal ID16043672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:36679011..36684290hg38UCSC Ensembl
Innerchr6:36646788..36652067hg19UCSC Ensembl
Innerchr6:36754766..36760045hg18UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg385280
hg195280
hg185280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10633n54
Supporting Variantsnssv1058383
Samples
Known GenesCDKN1A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602949
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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