A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380255



Internal ID21037808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:91277022..92377621hg38UCSC Ensembl
chr4:92198173..93298772hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg381100600
hg191100600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5362n223
Supporting Variantsnssv18215310
Samples
Known GenesCCSER1, GRID2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380255
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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