A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18087366



Internal ID20654406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:234704394..234705786hg38UCSC Ensembl
chr2:235613038..235614430hg19UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg381393
hg191393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6348887
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18087366
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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