A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983814



Internal ID18619006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:34692987..34694672hg38UCSC Ensembl
Innerchr14:35162193..35163878hg19UCSC Ensembl
Innerchr14:34231944..34233629hg18UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg381686
hg191686
hg181686
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1982101, nssv1982106, nssv1982103, nssv1982107, nssv1982100, nssv1982105, nssv1982102, nssv1982108, nssv1982104, nssv1982099
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)nsv983814
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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