A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960145



Internal ID18595398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:68117113..68162302hg38UCSC Ensembl
Innerchr17:66113254..66158443hg19UCSC Ensembl
Innerchr17:63624848..63670038hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3845190
hg1945190
hg1845191
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2109879, nssv2110676, nssv2109875, nssv2109880, nssv2109877, nssv2109882, nssv2109878, nssv2109883, nssv2109881, nssv2109876
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLINC00674
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960145
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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