A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2089428



Internal ID17486767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:31033387..31051069hg38UCSC Ensembl
Innerchr17:29360405..29378087hg19UCSC Ensembl
Innerchr17:26384531..26402213hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3817683
hg1917683
hg1817683
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv960088
Supporting Variants
SamplesHGDP00998
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Pab-Ppy-Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2089428
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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