A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18085937



Internal ID20652977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:33283684..33303598hg38UCSC Ensembl
chr2:33508751..33528665hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3819915
hg1919915
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6342172
Supporting Variants
Samples
Known GenesLTBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18085937
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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