A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215190



Internal ID20782230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181247451..181254112hg38UCSC Ensembl
chr5:180674451..180681112hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg386662
hg196662
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6402279
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215190
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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