A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18090589



Internal ID20657629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:60331896..60333067hg38UCSC Ensembl
chr2:60559031..60560202hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg381172
hg191172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6352944
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18090589
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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