A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2557759



Internal ID17393212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:87855517..87861341hg38UCSC Ensembl
Innerchr9:90470432..90476256hg19UCSC Ensembl
Innerchr9:89660252..89666076hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg385825
hg195825
hg185825
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv982317
Supporting Variants
SamplesHGDP00456
Known GenesLOC392364
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)nssv2557759
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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