A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18084395



Internal ID20651435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:203665702..203674488hg38UCSC Ensembl
chr2:204530425..204539211hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg388787
hg198787
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6354921
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18084395
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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