A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973616



Internal ID18608831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64396335..64397663hg38UCSC Ensembl
Innerchr9:43105459..43106777hg19UCSC Ensembl
Innerchr9:43095455..43096773hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg381329
hg191319
hg181319
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2732018, nssv2732020, nssv2732022, nssv2732055, nssv2732021, nssv2732057, nssv2732024, nssv2732054, nssv2732023, nssv2732056, nssv2732058, nssv2732025, nssv2732051, nssv2732053, nssv2732059, nssv2732026, nssv2732052, nssv2732019, nssv2732027, nssv2732060
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)nsv973616
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