A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560964



Internal ID333956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85012132..85014086hg38UCSC Ensembl
chr16:85045738..85047692hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg381955
hg191955
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17710253
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560964
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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