A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983854



Internal ID18272360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:100277697..100278585hg38UCSC Ensembl
Innerchr14:100744034..100744922hg19UCSC Ensembl
Innerchr14:99813787..99814675hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38889
hg19889
hg18889
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1997446, nssv1997443, nssv1997444, nssv1997442, nssv1997445, nssv1997449, nssv1997448, nssv1997447, nssv1997450, nssv1997451
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesYY1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv983854
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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