A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525573



Internal ID301729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:79707048..79777371hg38UCSC Ensembl
chr16:79740945..79811268hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3870324
hg1970324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17709570
Samples
Known GenesLOC101928248, LOC102467146
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525573
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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