A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048909



Internal ID18791440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:24438079..24465528hg38UCSC Ensembl
Innerchr13:25012217..25039666hg19UCSC Ensembl
Innerchr13:23910217..23937666hg18UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg3827450
hg1927450
hg1827450
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523164
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)nsv1048909
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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