A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2559307



Internal ID17818109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:94546455..94557929hg38UCSC Ensembl
Innerchr9:97308737..97320211hg19UCSC Ensembl
Innerchr9:96348558..96360032hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3811475
hg1911475
hg1811475
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972786
Supporting Variants
SamplesHGDP00927
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)nssv2559307
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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