A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1058382



Internal ID15564882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:36679011..36684112hg38UCSC Ensembl
Innerchr6:36646788..36651889hg19UCSC Ensembl
Innerchr6:36754766..36759867hg18UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg385102
hg195102
hg185102
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602948
Supporting Variants
Samples
Known GenesCDKN1A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1058382
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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