A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2566236



Internal ID17752009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:125190068..125196501hg38UCSC Ensembl
Innerchr9:127952347..127958780hg19UCSC Ensembl
Innerchr9:126992168..126998601hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg386434
hg196434
hg186434
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv968752
Supporting Variants
SamplesHGDP00521
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)nssv2566236
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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