A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208592



Internal ID20775633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:168012601..168017300hg38UCSC Ensembl
chr3:167730389..167735088hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg384700
hg194700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6364246
Supporting Variants
Samples
Known GenesGOLIM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208592
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00201


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