A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962366



Internal ID18597610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:72742424..72743154hg38UCSC Ensembl
Innerchr17:70738563..70739293hg19UCSC Ensembl
Innerchr17:68250158..68250888hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38731
hg19731
hg18731
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2108932, nssv2108923, nssv2108925, nssv2108927, nssv2108926, nssv2108931, nssv2108924, nssv2108929, nssv2108930, nssv2108928
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSLC39A11
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv962366
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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