A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17735861



Internal ID159527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:127936249..127947705hg38UCSC Ensembl
chr8:128948495..128959951hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3811457
hg1911457
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557329
Supporting Variants
Samples
Known GenesPVT1, TMEM75
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17735861
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.001405


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