A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100262



Internal ID20667302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188567281..188567804hg38UCSC Ensembl
chr3:188285069..188285592hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6359703
Supporting Variants
Samples
Known GenesLPP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100262
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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