A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18118262



Internal ID20685302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:65203448..65230208hg38UCSC Ensembl
chr4:66069166..66095926hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3826761
hg1926761
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6392039
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18118262
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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