A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18113996



Internal ID20681036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2554317..2575627hg38UCSC Ensembl
chr4:2556044..2577354hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3821311
hg1921311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6371949
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18113996
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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