A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209202



Internal ID20776242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170000060..170178407hg38UCSC Ensembl
chr3:169717848..169896195hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38178348
hg19178348
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6375571
Supporting Variants
Samples
Known GenesGPR160, PHC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209202
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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