A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18113994



Internal ID20681034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2552501..2566200hg38UCSC Ensembl
chr4:2554228..2567927hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3813700
hg1913700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6362106
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18113994
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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