A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215318



Internal ID20782358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:91572455..92312865hg38UCSC Ensembl
chr4:92493606..93234016hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38740411
hg19740411
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6390479
Supporting Variants
Samples
Known GenesCCSER1, GRID2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215318
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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