A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2081509



Internal ID17851716
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 Flag1
Merged StatusS
Merged Variantsnsv962279
Supporting Variants
SamplesHGDP01029
Known GenesFBXW10
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2081509
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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