A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276456



Internal ID20485674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85208801..85208900hg38UCSC Ensembl
chr16:85242407..85242506hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731354
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276456
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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