A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17633770



Internal ID21825817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63415308..63415845hg38UCSC Ensembl
chr18:61082541..61083078hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38538
hg19538
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6024547
Supporting Variants
Samples
Known GenesVPS4B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17633770
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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