A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2561167



Internal ID17779309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:97199777..97221161hg38UCSC Ensembl
Innerchr9:99962059..99983443hg19UCSC Ensembl
Innerchr9:99001880..99023264hg18UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3821385
hg1921385
hg1821385
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972433
Supporting Variants
SamplesHGDP00665
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)nssv2561167
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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