A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215891



Internal ID20782931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:155729833..156136944hg38UCSC Ensembl
chr5:155109393..155563954hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38407112
hg19454562
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6398780
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215891
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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