A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974374



Internal ID18609585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103146896..103149400hg38UCSC Ensembl
Innerchr14:103613233..103615737hg19UCSC Ensembl
Innerchr14:102682986..102685490hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg382505
hg192505
hg182505
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1998517, nssv1998516, nssv1998518, nssv1998524, nssv1998522, nssv1998525, nssv1998523, nssv1998519, nssv1998521, nssv1998520
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)nsv974374
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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