A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035266



Internal ID18777797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:23163833..23180307hg38UCSC Ensembl
Innerchr13:23737972..23754446hg19UCSC Ensembl
Innerchr13:22635972..22652446hg18UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg3816475
hg1916475
hg1816475
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523155, nssv3523154
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)nsv1035266
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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