A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1860732



Internal ID17390686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87965292..87966480hg38UCSC Ensembl
Innerchr10:89725049..89726237hg19UCSC Ensembl
Innerchr10:89715029..89716217hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg381189
hg191189
hg181189
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948128
Supporting Variants
SamplesHGDP00456
Known GenesPTEN
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)nssv1860732
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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