A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220108



Internal ID20787148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30675384..30680515hg38UCSC Ensembl
chr8:30532901..30538032hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg385132
hg195132
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6433149
Supporting Variants
Samples
Known GenesGSR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220108
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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