A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17017237



Internal ID79151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:130393596..130482687hg38UCSC Ensembl
chr8:131405842..131494933hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3889092
hg1989092
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557690
Supporting Variants
Samples
Known GenesASAP1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17017237
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000468


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