A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042921



Internal ID19132140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63747736..63831177hg38UCSC Ensembl
Innerchr13:64321869..64405310hg19UCSC Ensembl
Innerchr13:63219870..63303311hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3883442
hg1983442
hg1883442
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1692n100
Supporting Variantsnssv3526727, nssv3711806, nssv3711807, nssv3526725, nssv3711808, nssv3526726
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)nsv1042921
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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