A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18111959



Internal ID20678999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1515801..1518686hg38UCSC Ensembl
chr4:1517528..1520413hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg382886
hg192886
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6361694
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18111959
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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