A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18086898



Internal ID20653938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:53669801..53721300hg38UCSC Ensembl
chr2:53896938..53948437hg19UCSC Ensembl
Cytoband2p16.2
Allele length
AssemblyAllele length
hg3851500
hg1951500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6337968
Supporting Variants
Samples
Known GenesASB3, GPR75-ASB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18086898
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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