A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360468



Internal ID21018021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3672665..3743704hg38UCSC Ensembl
chr4:3674392..3745431hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3871040
hg1971040
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213546
Samples
Known GenesLOC100133461
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360468
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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