A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038853



Internal ID19128072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63458003..63495866hg38UCSC Ensembl
Innerchr13:64032136..64069999hg19UCSC Ensembl
Innerchr13:62930137..62968000hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3837864
hg1937864
hg1837864
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1684n100
Supporting Variantsnssv3711770
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)nsv1038853
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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