A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523172



Internal ID18474767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:24445874..24465528hg38UCSC Ensembl
Innerchr13:25020012..25039666hg19UCSC Ensembl
Innerchr13:23918012..23937666hg18UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg3819655
hg1919655
hg1819655
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044637
Supporting Variants
Samples
Known GenesPARP4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3523172
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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