A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3481065



Internal ID18722829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:3627619..3769754hg38UCSC Ensembl
Innerchr1:3544183..3686318hg19UCSC Ensembl
Innerchr1:3534043..3676178hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38142136
hg19142136
hg18142136
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001715
Supporting Variants
Samples
Known GenesCCDC27, TP73, TP73-AS1, TPRG1L, WRAP73
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3481065
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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