A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18119038



Internal ID20686078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:69880488..69891157hg38UCSC Ensembl
chr4:70746206..70756875hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3810670
hg1910670
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6392244
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18119038
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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