A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18127117



Internal ID20694157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132153146..132156031hg38UCSC Ensembl
chr5:131488839..131491724hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg382886
hg192886
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6408099
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18127117
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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