A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2559207



Internal ID17775334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:94481483..94492314hg38UCSC Ensembl
Innerchr9:97243765..97254596hg19UCSC Ensembl
Innerchr9:96283586..96294417hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3810832
hg1910832
hg1810832
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972423
Supporting Variants
SamplesHGDP00542
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)nssv2559207
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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