A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18113736



Internal ID20680776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16292501..16302100hg38UCSC Ensembl
chr4:16294124..16303723hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg389600
hg199600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6362500
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18113736
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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