A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18091666



Internal ID20658706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:97829937..98099276hg38UCSC Ensembl
chr2:98446400..98715739hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38269340
hg19269340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6350757
Supporting Variants
Samples
Known GenesTMEM131, VWA3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18091666
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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