A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213895



Internal ID20780935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:152236095..152241957hg38UCSC Ensembl
chr5:151615656..151621518hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg385863
hg195863
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411250
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213895
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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