A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2551299



Internal ID17740197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65737118..65768709hg38UCSC Ensembl
Innerchr9:70397336..70428927hg19UCSC Ensembl
Innerchr9:69637156..69668747hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3831592
hg1931592
hg1831592
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv982298
Supporting Variants
SamplesHGDP00456
Known GenesFOXD4L2, FOXD4L4
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)nssv2551299
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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