A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974385



Internal ID18609596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:106866254..106881350hg38UCSC Ensembl
Innerchr14:107274469..107289540hg19UCSC Ensembl
Innerchr14:106345514..106360674hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3815097
hg1915072
hg1815161
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2002844, nssv2002571, nssv2002839, nssv2002837, nssv2002843, nssv2002842, nssv2002841, nssv2002838, nssv2002840, nssv2002572
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)nsv974385
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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