A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545129



Internal ID15985852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:3680453..3755227hg38UCSC Ensembl
Innerchr1:3597017..3671791hg19UCSC Ensembl
Innerchr1:3586877..3661651hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3874775
hg1974775
hg1874775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1172590
SamplesHGDP00787
Known GenesCCDC27, TP73, TP73-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545129
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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