A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038671



Internal ID18781202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:24449798..24465528hg38UCSC Ensembl
Innerchr13:25023936..25039666hg19UCSC Ensembl
Innerchr13:23921936..23937666hg18UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg3815731
hg1915731
hg1815731
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1617n100
Supporting Variantsnssv3523181, nssv3523178, nssv3523182, nssv3523179, nssv3523180
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)nsv1038671
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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