A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18090074



Internal ID20657114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:66661979..66666923hg38UCSC Ensembl
chr2:66889111..66894055hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg384945
hg194945
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6337230
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18090074
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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