A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18118040



Internal ID20685080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:59208663..59210302hg38UCSC Ensembl
chr4:60074381..60076020hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg381640
hg191640
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6385959
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18118040
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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