A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18149782



Internal ID20716822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:95323701..95326000hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6403150
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18149782
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0008


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