A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362493



Internal ID21020046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2445793..2508352hg38UCSC Ensembl
chr4:2447520..2510079hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3862560
hg1962560
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211782
Samples
Known GenesLOC402160, RNF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362493
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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