A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983858



Internal ID18619050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103240555..103244753hg38UCSC Ensembl
Innerchr14:103706892..103711090hg19UCSC Ensembl
Innerchr14:102776645..102780843hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg384199
hg194199
hg184199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1997108, nssv1997113, nssv1997111, nssv1997115, nssv1997109, nssv1997114, nssv1997116, nssv1997110, nssv1997107, nssv1997112
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)nsv983858
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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