A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960521



Internal ID18249086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:64946159..64957699hg38UCSC Ensembl
Innerchr17:62942277..62953817hg19UCSC Ensembl
Innerchr17:60372739..60384279hg18UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg3811541
hg1911541
hg1811541
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2108407, nssv2108403, nssv2108400, nssv2108404, nssv2108401, nssv2108406, nssv2108399, nssv2108398, nssv2108402, nssv2108405
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)nsv960521
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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