A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18126651



Internal ID20693691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:162015590..162015966hg38UCSC Ensembl
chr5:161442596..161442972hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38377
hg19377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6401568
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18126651
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00115


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