A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5526471



Internal ID302599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75599225..75623878hg38UCSC Ensembl
chr16:75633123..75657776hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3824654
hg1924654
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17709129
Samples
Known GenesADAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5526471
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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