A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211619



Internal ID20778659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6651201..6698200hg38UCSC Ensembl
chr4:6652928..6699927hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3847000
hg1947000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6362639
Supporting Variants
Samples
Known GenesLOC93622, S100P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211619
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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