A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745173



Internal ID20521178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20820503..20820651hg38UCSC Ensembl
chr16:20831825..20831973hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16284113
Samples
Known GenesLOC81691
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745173
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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