A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977496



Internal ID18612702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:89734863..89740477hg38UCSC Ensembl
Innerchr14:90201207..90206821hg19UCSC Ensembl
Innerchr14:89270960..89276574hg18UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg385615
hg195615
hg185615
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1995392, nssv1995394, nssv1995395, nssv1995396, nssv1995393, nssv1995400, nssv1995398, nssv1995401, nssv1995397, nssv1995399
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)nsv977496
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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