A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18126402



Internal ID20693442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:119828588..119857167hg38UCSC Ensembl
chr5:119164283..119192862hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3828580
hg1928580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6403862
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18126402
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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