A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18085814



Internal ID20652854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:217206280..217233668hg38UCSC Ensembl
chr2:218071003..218098391hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3827389
hg1927389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6350143
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18085814
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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