A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18086449



Internal ID20653489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:39637038..39644016hg38UCSC Ensembl
chr2:39864178..39871156hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg386979
hg196979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6337636
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18086449
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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