A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562592



Internal ID335541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:25619922..25620160hg38UCSC Ensembl
chr16:25631243..25631481hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17706628
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562592
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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