A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17624951



Internal ID21816998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:33096297..33096354hg38UCSC Ensembl
chr18:30676261..30676318hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036856
Supporting Variants
Samples
Known GenesCCDC178
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17624951
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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