A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982493



Internal ID18617688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:67890585..67891558hg38UCSC Ensembl
Innerchr9:67958031..67959004hg19UCSC Ensembl
Innerchr9:67547851..67548824hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38974
hg19974
hg18974
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2740719, nssv2740715, nssv2739856, nssv2739859, nssv2739851, nssv2739858, nssv2740713, nssv2740720, nssv2739853, nssv2740717, nssv2740712, nssv2739854, nssv2740716, nssv2740718, nssv2740721, nssv2740714, nssv2739850, nssv2739857, nssv2739855, nssv2739852
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)nsv982493
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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