A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044100



Internal ID19133319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63770336..63845046hg38UCSC Ensembl
Innerchr13:64344469..64419179hg19UCSC Ensembl
Innerchr13:63242470..63317180hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3874711
hg1974711
hg1874711
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1692n100
Supporting Variantsnssv3526790, nssv3526789
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)nsv1044100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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