A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18118364



Internal ID20685404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55478039..55478695hg38UCSC Ensembl
chr4:56344206..56344862hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38657
hg19657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6376771
Supporting Variants
Samples
Known GenesCLOCK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18118364
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00045


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