A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17635461



Internal ID21827508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:50240209..50240290hg38UCSC Ensembl
chr18:47766579..47766660hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6026371
Supporting Variants
Samples
Known GenesCCDC11
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17635461
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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