A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2559596



Internal ID17505567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:95293068..95294753hg38UCSC Ensembl
Innerchr9:98055350..98057035hg19UCSC Ensembl
Innerchr9:97095171..97096856hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg381686
hg191686
hg181686
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972787
Supporting Variants
SamplesHGDP01029
Known GenesFANCC
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)nssv2559596
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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