A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982338



Internal ID18270847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113106108..113111873hg38UCSC Ensembl
Innerchr9:115868388..115874153hg19UCSC Ensembl
Innerchr9:114908209..114913974hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg385766
hg195766
hg185766
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2565813, nssv2565816, nssv2565814, nssv2565822, nssv2565821, nssv2565815, nssv2565817, nssv2565819, nssv2565820, nssv2565818
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFAM225B
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982338
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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