A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18090994



Internal ID20658034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:79398601..79403400hg38UCSC Ensembl
chr2:79625727..79630526hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg384800
hg194800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6338094
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18090994
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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