A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214767



Internal ID20781807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:88004301..88007200hg38UCSC Ensembl
chr4:88925453..88928352hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6394406
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214767
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00048


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