A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18089442



Internal ID20656482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:60858350..60879092hg38UCSC Ensembl
chr2:61085485..61106227hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3820743
hg1920743
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6351355
Supporting Variants
Samples
Known GenesFLJ16341
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18089442
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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