A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6394589



Internal ID21052142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:91313848..91375237hg38UCSC Ensembl
chr4:92234999..92296388hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3861390
hg1961390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18119970
Samples
Known GenesCCSER1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6394589
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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