A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18088690



Internal ID20655730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:44956024..44961501hg38UCSC Ensembl
chr2:45183163..45188640hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg385478
hg195478
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6337506
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18088690
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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