A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18089366



Internal ID20656406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:46865610..46866237hg38UCSC Ensembl
chr2:47092749..47093376hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38628
hg19628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6341351
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18089366
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00027


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