A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2560275



Internal ID17496263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:96499186..96503444hg38UCSC Ensembl
Innerchr9:99261468..99265726hg19UCSC Ensembl
Innerchr9:98301289..98305547hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg384259
hg194259
hg184259
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv968737
Supporting Variants
SamplesHGDP01029
Known GenesCDC14B
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)nssv2560275
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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