A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18089966



Internal ID20657006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65325960..65328285hg38UCSC Ensembl
chr2:65553094..65555419hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg382326
hg192326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6346780
Supporting Variants
Samples
Known GenesSPRED2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18089966
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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