A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982425



Internal ID18617620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64383612..64387553hg38UCSC Ensembl
Innerchr9:43115543..43119485hg19UCSC Ensembl
Innerchr9:43105539..43109481hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg383942
hg193943
hg183943
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2733407, nssv2733411, nssv2733464, nssv2733465, nssv2733472, nssv2733467, nssv2733406, nssv2733468, nssv2733473, nssv2733466, nssv2733469, nssv2733413, nssv2733470, nssv2733471, nssv2733405, nssv2733410, nssv2733412, nssv2733409, nssv2733408, nssv2733414
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982425
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer