A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2559708



Internal ID17539003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:94038022..94039417hg38UCSC Ensembl
Innerchr9:96800304..96801699hg19UCSC Ensembl
Innerchr9:95840125..95841520hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg381396
hg191396
hg181396
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv982322
Supporting Variants
SamplesHGDP01307
Known GenesPTPDC1
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)nssv2559708
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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