A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047902



Internal ID19137121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:95292864..95380575hg38UCSC Ensembl
Innerchr13:95945118..96032829hg19UCSC Ensembl
Innerchr13:94743119..94830830hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3887712
hg1987712
hg1887712
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1731n100
Supporting Variantsnssv3525508, nssv3525507
Samples
Known GenesABCC4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047902
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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