A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18086563



Internal ID20653604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:231209366..231212878hg38UCSC Ensembl
chr2:232074079..232077591hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg383513
hg193513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6343376
Supporting Variants
Samples
Known GenesARMC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18086563
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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