A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983838



Internal ID18619030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:67799292..67800092hg38UCSC Ensembl
Innerchr14:68266009..68266809hg19UCSC Ensembl
Innerchr14:67335762..67336562hg18UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg38801
hg19801
hg18801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1990880, nssv1990882, nssv1990881, nssv1990874, nssv1990876, nssv1990878, nssv1990883, nssv1990877, nssv1990875, nssv1990879
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZFYVE26
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv983838
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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