A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969573



Internal ID18604800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64398925..64402003hg38UCSC Ensembl
Innerchr9:43101115..43104198hg19UCSC Ensembl
Innerchr9:43091111..43094194hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg383079
hg193084
hg183084
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2731726, nssv2731723, nssv2731722, nssv2731724, nssv2731728, nssv2731731, nssv2731730, nssv2731727, nssv2731729, nssv2731725
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)nsv969573
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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