A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972407



Internal ID18260937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:83886982..83902905hg38UCSC Ensembl
Innerchr9:86501897..86517820hg19UCSC Ensembl
Innerchr9:85691717..85707640hg18UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3815924
hg1915924
hg1815924
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2555495, nssv2555498, nssv2555501, nssv2555493, nssv2555492, nssv2555494, nssv2555496, nssv2555497, nssv2555499, nssv2555500
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesKIF27
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972407
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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