A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18126782



Internal ID20693822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:153828223..153833220hg38UCSC Ensembl
chr5:153207783..153212780hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg384998
hg194998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411162
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18126782
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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