A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211925



Internal ID20778965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:54062901..54065600hg38UCSC Ensembl
chr4:54929068..54931767hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6383236
Supporting Variants
Samples
Known GenesCHIC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211925
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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