A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960150



Internal ID18595403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:80541525..80543233hg38UCSC Ensembl
Innerchr17:78515325..78517033hg19UCSC Ensembl
Innerchr17:76129920..76131628hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg381709
hg191709
hg181709
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2112850, nssv2112848, nssv2112847, nssv2112841, nssv2112849, nssv2112845, nssv2112844, nssv2112843, nssv2112846, nssv2112842
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)nsv960150
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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