A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2086809



Internal ID17786804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:26982040..27007049hg38UCSC Ensembl
Innerchr17:25309066..25334075hg19UCSC Ensembl
Innerchr17:22333193..22358202hg18UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg3825010
hg1925010
hg1825010
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv960449
Supporting Variants
SamplesHGDP00665
Known Genes
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)nssv2086809
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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