A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973617



Internal ID18608832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64393756..64395637hg38UCSC Ensembl
Innerchr9:43107475..43109340hg19UCSC Ensembl
Innerchr9:43097471..43099336hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg381882
hg191866
hg181866
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2733089, nssv2732229, nssv2733082, nssv2732228, nssv2732224, nssv2732223, nssv2733091, nssv2732231, nssv2733073, nssv2733093, nssv2733075, nssv2732227, nssv2733086, nssv2732230, nssv2732226, nssv2733078, nssv2733079, nssv2733076, nssv2732232, nssv2733077, nssv2733080, nssv2733081, nssv2733084, nssv2733088, nssv2733090, nssv2733092, nssv2732225, nssv2733087, nssv2733074, nssv2733085
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)nsv973617
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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