A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052702



Internal ID19141921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:97775552..97932141hg38UCSC Ensembl
Innerchr13:98427806..98584395hg19UCSC Ensembl
Innerchr13:97225807..97382396hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg38156590
hg19156590
hg18156590
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525519, nssv3525520
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052702
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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