A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215943



Internal ID20782983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161240201..161248900hg38UCSC Ensembl
chr5:160667208..160675907hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg388700
hg198700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6405351
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215943
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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