A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983805



Internal ID18618997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22669230..22695643hg38UCSC Ensembl
Innerchr14:23138439..23164852hg19UCSC Ensembl
Innerchr14:22208279..22234692hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3826414
hg1926414
hg1826414
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1979964, nssv1979967, nssv1979969, nssv1979961, nssv1979960, nssv1979968, nssv1979963, nssv1979965, nssv1979962, nssv1979966
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)nsv983805
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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