A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962279



Internal ID18597523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:18740326..18771650hg38UCSC Ensembl
Innerchr17:18643639..18674963hg19UCSC Ensembl
Innerchr17:18584364..18615688hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3831325
hg1931325
hg1831325
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2081509, nssv2081511, nssv2081504, nssv2081507, nssv2081506, nssv2081505, nssv2081508, nssv2081503, nssv2081510, nssv2081502
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFBXW10
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv962279
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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