A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208341



Internal ID20775381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:235361091..235669534hg38UCSC Ensembl
chr2:236269735..236578178hg19UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg38308444
hg19308444
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6352540
Supporting Variants
Samples
Known GenesAGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208341
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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