A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969572



Internal ID18604799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64402003..64403607hg38UCSC Ensembl
Innerchr9:43099507..43101115hg19UCSC Ensembl
Innerchr9:43089503..43091111hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg381605
hg191609
hg181609
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2731651, nssv2731597, nssv2731652, nssv2731654, nssv2731602, nssv2731593, nssv2731658, nssv2731596, nssv2731660, nssv2731659, nssv2731653, nssv2731599, nssv2731595, nssv2731594, nssv2731656, nssv2731598, nssv2731601, nssv2731657, nssv2731655, nssv2731600
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)nsv969572
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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