A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733271



Internal ID156937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57000079..57004690hg38UCSC Ensembl
chr20:55575135..55579746hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg384612
hg194612
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557328
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733271
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000781


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