A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17542252



Internal ID21866607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186252608..186252686hg38UCSC Ensembl
chr4:187173762..187173840hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5996143
Supporting Variants
Samples
Known GenesKLKB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17542252
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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