A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973205



Internal ID18608420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33566606..33567344hg38UCSC Ensembl
Innerchr9:33566604..33567342hg19UCSC Ensembl
Innerchr9:33556604..33557342hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38739
hg19739
hg18739
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2722950, nssv2722946, nssv2722949, nssv2722945, nssv2722948, nssv2722947, nssv2722953, nssv2722954, nssv2722952, nssv2722951
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD18B
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv973205
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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