A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210362



Internal ID20777402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157117001..157122800hg38UCSC Ensembl
chr3:156834790..156840589hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg385800
hg195800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6358733
Supporting Variants
Samples
Known GenesLINC00880
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210362
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00018


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