A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203830



Internal ID20770870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11833801..11837900hg38UCSC Ensembl
chr4:49264871..49268886hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg384100
hg194016
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6535905
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203830
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.08258


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