A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17720539



Internal ID144205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3144551..3144705hg38UCSC Ensembl
chr19:3144549..3144703hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558340
Supporting Variants
Samples
Known GenesGNA15
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17720539
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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