A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6144522



Internal ID343727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20820508..20820651hg38UCSC Ensembl
chr16:20831830..20831973hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704749
Samples
Known GenesLOC81691
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6144522
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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