A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973244



Internal ID18608459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:40247551..40249430hg38UCSC Ensembl
Innerchr9:42392569..42394448hg19UCSC Ensembl
Innerchr9:42382565..42384444hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg381880
hg191880
hg181880
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2727688, nssv2727682, nssv2727687, nssv2727689, nssv2727685, nssv2727690, nssv2727691, nssv2727684, nssv2727683, nssv2727686
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)nsv973244
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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