A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18089900



Internal ID20656940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:41142411..41153080hg38UCSC Ensembl
chr2:41369551..41380220hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3810670
hg1910670
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6346920
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18089900
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00049


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