A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982278



Internal ID18617473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:66658902..66721645hg38UCSC Ensembl
Innerchr9:65996308..66059051hg19UCSC Ensembl
Innerchr9:65736128..65798871hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3862744
hg1962744
hg1862744
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2545793, nssv2545799, nssv2545801, nssv2545800, nssv2545798, nssv2545797, nssv2545796, nssv2545794, nssv2545792, nssv2545795
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)nsv982278
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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