A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18108057



Internal ID20675097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139620618..139621016hg38UCSC Ensembl
chr4:140541772..140542170hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg38399
hg19399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6384840
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18108057
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00147


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