A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206642



Internal ID20773682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:141750076..141790862hg38UCSC Ensembl
chr2:142507645..142548431hg19UCSC Ensembl
Cytoband2q22.2
Allele length
AssemblyAllele length
hg3840787
hg1940787
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6341603
Supporting Variants
Samples
Known GenesLRP1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206642
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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