A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982490



Internal ID18617685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42860687..42863840hg38UCSC Ensembl
Innerchr9:67934873..67938033hg19UCSC Ensembl
Innerchr9:67524693..67527853hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg383154
hg193161
hg183161
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2740039, nssv2740043, nssv2740041, nssv2740036, nssv2740040, nssv2740037, nssv2740038, nssv2740034, nssv2740042, nssv2740035
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD20A1, ANKRD20A3
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982490
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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