A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972792



Internal ID18261322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:97698069..97704083hg38UCSC Ensembl
Innerchr9:100460351..100466365hg19UCSC Ensembl
Innerchr9:99500172..99506186hg18UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg386015
hg196015
hg186015
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2563732, nssv2563737, nssv2563738, nssv2563734, nssv2563731, nssv2563735, nssv2563733, nssv2563736, nssv2563729, nssv2563730
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972792
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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