A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213566



Internal ID20780606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3883949..4151110hg38UCSC Ensembl
chr4:3885676..4152837hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38267162
hg19267162
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6371566
Supporting Variants
Samples
Known GenesFAM86EP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213566
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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