A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981111



Internal ID18269624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:25022970..25024663hg38UCSC Ensembl
Innerchr6:25023198..25024891hg19UCSC Ensembl
Innerchr6:25131177..25132870hg18UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg381694
hg191694
hg181694
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2395525, nssv2395520, nssv2395518, nssv2395517, nssv2395516, nssv2395519, nssv2395522, nssv2395523, nssv2395524, nssv2395521
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesFAM65B
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981111
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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