A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983835



Internal ID18619027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:65265742..65268652hg38UCSC Ensembl
Innerchr14:65732460..65735370hg19UCSC Ensembl
Innerchr14:64802213..64805123hg18UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg382911
hg192911
hg182911
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1990455, nssv1990452, nssv1990454, nssv1990449, nssv1990448, nssv1990446, nssv1990447, nssv1990453, nssv1990451, nssv1990450
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv983835
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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