A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16261025



Internal ID20470243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45749762..45750001hg38UCSC Ensembl
chr19:46253020..46253259hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38240
hg19240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4746258
Supporting Variants
Samples
Known GenesLOC388553
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16261025
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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