A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18127071



Internal ID20694111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:153032432..153036241hg38UCSC Ensembl
chr5:152411992..152415801hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg383810
hg193810
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6402746
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18127071
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00033


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