A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973346



Internal ID18608561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64400855..64403713hg38UCSC Ensembl
Innerchr9:69413273..69416131hg19UCSC Ensembl
Innerchr9:68703093..68705951hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg382859
hg192859
hg182859
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2744658, nssv2743802, nssv2743799, nssv2743797, nssv2743795, nssv2744662, nssv2744659, nssv2743800, nssv2743796, nssv2744656, nssv2744655, nssv2744664, nssv2744660, nssv2744657, nssv2743798, nssv2744663, nssv2744661, nssv2743801, nssv2743794, nssv2743793
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD20A4
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv973346
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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