A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260194



Internal ID20469412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57218716..57219039hg38UCSC Ensembl
chr16:57252628..57252951hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4745891
Supporting Variants
Samples
Known GenesRSPRY1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260194
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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