A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18112874



Internal ID20679914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15063367..15063800hg38UCSC Ensembl
chr4:15064991..15065424hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38434
hg19434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6375424
Supporting Variants
Samples
Known GenesCPEB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18112874
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00112


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