A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977485



Internal ID18612691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:74369047..74386435hg38UCSC Ensembl
Innerchr14:74835750..74853138hg19UCSC Ensembl
Innerchr14:73905503..73922891hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3817389
hg1917389
hg1817389
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1993600, nssv1993599, nssv1993604, nssv1993603, nssv1993607, nssv1993605, nssv1993601, nssv1993606, nssv1993598, nssv1993602
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)nsv977485
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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