A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373287



Internal ID21030840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:4621422..4641556hg38UCSC Ensembl
chr4:4623149..4643283hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3820135
hg1920135
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213700
Samples
Known GenesSTX18-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373287
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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