A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212741



Internal ID20779781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:157244341..157302637hg38UCSC Ensembl
chr4:158165493..158223789hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3858297
hg1958297
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6376989
Supporting Variants
Samples
Known GenesGRIA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212741
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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