A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976363



Internal ID18264883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:89156118..89159980hg38UCSC Ensembl
Innerchr14:89622462..89626324hg19UCSC Ensembl
Innerchr14:88692215..88696077hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg383863
hg193863
hg183863
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1994028, nssv1994027, nssv1994030, nssv1994025, nssv1994026, nssv1994033, nssv1994029, nssv1994031, nssv1994034, nssv1994032
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesFOXN3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976363
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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