A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556428



Internal ID329565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24392682..24394225hg38UCSC Ensembl
chr16:24404003..24405546hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg381544
hg191544
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17706551
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556428
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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