A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703983



Internal ID127649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69977138..69977185hg38UCSC Ensembl
chr15:70269477..70269524hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3848
hg1948
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555582
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703983
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000468


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