A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2566838



Internal ID17539733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:132960189..132966468hg38UCSC Ensembl
Innerchr9:135835576..135841855hg19UCSC Ensembl
Innerchr9:134825397..134831676hg18UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg386280
hg196280
hg186280
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972809
Supporting Variants
SamplesHGDP01307
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)nssv2566838
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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