A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037251



Internal ID18779782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:111024367..111092439hg38UCSC Ensembl
Innerchr13:111676714..111744786hg19UCSC Ensembl
Innerchr13:110474715..110542787hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3868073
hg1968073
hg1868073
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1742n100
Supporting Variantsnssv3525589
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)nsv1037251
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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