A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208962



Internal ID20776002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:131384002..132144415hg38UCSC Ensembl
chr3:131102846..131863259hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38760414
hg19760414
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6369922
Supporting Variants
Samples
Known GenesCPNE4, MIR5704, MRPL3, NUDT16, SNORA58
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208962
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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