A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973684



Internal ID18608899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63065731..63110185hg38UCSC Ensembl
Innerchr9:66970703..67015157hg19UCSC Ensembl
Innerchr9:66710523..66754977hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3844455
hg1944455
hg1844455
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2737819, nssv2737785, nssv2737820, nssv2737823, nssv2737821, nssv2737818, nssv2737816, nssv2737817, nssv2737782, nssv2737781, nssv2737789, nssv2737788, nssv2737786, nssv2737815, nssv2737783, nssv2737784, nssv2737814, nssv2737780, nssv2737787, nssv2737822
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv973684
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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