A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18122839



Internal ID20689879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:115124538..115125254hg38UCSC Ensembl
chr5:114460235..114460951hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg38717
hg19717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6409460
Supporting Variants
Samples
Known GenesTRIM36
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18122839
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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