A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18118039



Internal ID20685079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:59208355..59217708hg38UCSC Ensembl
chr4:60074073..60083426hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg389354
hg199354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6381900
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18118039
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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