A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036163



Internal ID19125382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:55946305..55968359hg38UCSC Ensembl
Innerchr14:56413023..56435077hg19UCSC Ensembl
Innerchr14:55482776..55504830hg18UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3822055
hg1922055
hg1822055
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1922n100
Supporting Variantsnssv3531032
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)nsv1036163
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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