A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2566937



Internal ID17462773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133009500..133022589hg38UCSC Ensembl
Innerchr9:135884887..135897976hg19UCSC Ensembl
Innerchr9:134874708..134887797hg18UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3813090
hg1913090
hg1813090
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972810
Supporting Variants
SamplesHGDP00778
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)nssv2566937
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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