A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100032



Internal ID20667072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33115030..33135621hg38UCSC Ensembl
chr3:33156522..33177113hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3820592
hg1920592
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6364168
Supporting Variants
Samples
Known GenesCRTAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100032
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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