A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211658



Internal ID20778698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:69060508..69062987hg38UCSC Ensembl
chr4:69926226..69928705hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg382480
hg192480
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6378737
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211658
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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