A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032768



Internal ID21942111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57218709..57219032hg38UCSC Ensembl
chr16:57252621..57252944hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623030
Samples
Known GenesRSPRY1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032768
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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