A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376083



Internal ID21033636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42888084..42930402hg38UCSC Ensembl
chr4:42890101..42932419hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3842319
hg1942319
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213650
Samples
Known GenesGRXCR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376083
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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