A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983815



Internal ID18619007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35818518..35821007hg38UCSC Ensembl
Innerchr14:36287724..36290213hg19UCSC Ensembl
Innerchr14:35357475..35359964hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg382490
hg192490
hg182490
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1982654, nssv1982652, nssv1982661, nssv1982660, nssv1982656, nssv1982657, nssv1982653, nssv1982659, nssv1982658, nssv1982655
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)nsv983815
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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