A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046663



Internal ID19135882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113140947..113185654hg38UCSC Ensembl
Innerchr13:113795261..113839968hg19UCSC Ensembl
Innerchr13:112843262..112887969hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3844708
hg1944708
hg1844708
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525619
Samples
Known GenesF10, PCID2, PROZ
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046663
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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