A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039613



Internal ID19128832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:106779223..106877229hg38UCSC Ensembl
Innerchr14:107187462..107285437hg19UCSC Ensembl
Innerchr14:106258507..106356482hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3898007
hg1997976
hg1897976
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2165n100
Supporting Variantsnssv3534382
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)nsv1039613
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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