A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971615



Internal ID18606832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:407930..411010hg38UCSC Ensembl
Innerchr8:357930..361010hg19UCSC Ensembl
Innerchr8:347930..351010hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg383081
hg193081
hg183081
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2490014, nssv2490022, nssv2490023, nssv2490020, nssv2490019, nssv2490018, nssv2490017, nssv2490016, nssv2490021, nssv2490015
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFBXO25
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv971615
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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