A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18090091



Internal ID20657131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:66817062..66826509hg38UCSC Ensembl
chr2:67044194..67053641hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg389448
hg199448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6345372
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18090091
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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