A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969548



Internal ID18604775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:40258383..40258979hg38UCSC Ensembl
Innerchr9:42403401..42403997hg19UCSC Ensembl
Innerchr9:42393397..42393993hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38597
hg19597
hg18597
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2726835, nssv2726894, nssv2726831, nssv2726891, nssv2726892, nssv2726890, nssv2726833, nssv2726893, nssv2726897, nssv2726830, nssv2726839, nssv2726834, nssv2726888, nssv2726889, nssv2726895, nssv2726836, nssv2726832, nssv2726896, nssv2726838, nssv2726837
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)nsv969548
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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