A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099687



Internal ID20666727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177269084..177274610hg38UCSC Ensembl
chr3:176986872..176992398hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg385527
hg195527
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6362607
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099687
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00028


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