A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18097559



Internal ID20664599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183697601..183698100hg38UCSC Ensembl
chr3:183415389..183415888hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6358083
Supporting Variants
Samples
Known GenesYEATS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18097559
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.07214


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