A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18116683



Internal ID20683723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:32583992..32584562hg38UCSC Ensembl
chr4:32585614..32586184hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38571
hg19571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357219
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18116683
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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