A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16984938



Internal ID57347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:50624389..50631006hg38UCSC Ensembl
chr6:50592102..50598719hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg386618
hg196618
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555259
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16984938
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.01764


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