A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2557659



Internal ID17805200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:87838138..87853377hg38UCSC Ensembl
Innerchr9:90453053..90468292hg19UCSC Ensembl
Innerchr9:89642873..89658112hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3815240
hg1915240
hg1815240
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv968719
Supporting Variants
SamplesHGDP00778
Known GenesCTSLP8
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)nssv2557659
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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