A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215305



Internal ID20782345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:91168406..92461941hg38UCSC Ensembl
chr4:92089557..93383092hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg381293536
hg191293536
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6380980
Supporting Variants
Samples
Known GenesCCSER1, GRID2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215305
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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