A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18080171



Internal ID20647211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:162153085..162161548hg38UCSC Ensembl
chr2:163009595..163018058hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg388464
hg198464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6342924
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18080171
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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