A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5527879



Internal ID303959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:71800136..71805762hg38UCSC Ensembl
chr16:71834039..71839665hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg385627
hg195627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17708589
Samples
Known GenesAP1G1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5527879
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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