A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001715



Internal ID19090932
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 StatusM
Merged Variants
Supporting Variantsnssv3481065
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)nsv1001715
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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