A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18123831



Internal ID20690872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:114644817..114718168hg38UCSC Ensembl
chr5:113980514..114053865hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3873352
hg1973352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6410712
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18123831
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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