A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18084561



Internal ID20651601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:24080226..24090413hg38UCSC Ensembl
chr2:24303096..24313283hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3810188
hg1910188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6351148
Supporting Variants
Samples
Known GenesTP53I3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18084561
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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