A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973709



Internal ID18608924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64359160..64370145hg38UCSC Ensembl
Innerchr9:69371578..69382563hg19UCSC Ensembl
Innerchr9:68661398..68672383hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3810986
hg1910986
hg1810986
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2743449, nssv2743476, nssv2743446, nssv2743395, nssv2743475, nssv2743451, nssv2743481, nssv2743448, nssv2743399, nssv2743402, nssv2743443, nssv2743445, nssv2743479, nssv2743444, nssv2743403, nssv2743482, nssv2743484, nssv2743477, nssv2743401, nssv2743396, nssv2743400, nssv2743394, nssv2743447, nssv2743450, nssv2743483, nssv2743480, nssv2743478, nssv2743397, nssv2743442, nssv2743398
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)nsv973709
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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