A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206079



Internal ID20773119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:19416521..20093799hg38UCSC Ensembl
chr2:19616282..20293560hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38677279
hg19677279
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6340945
Supporting Variants
Samples
Known GenesLAPTM4A, LINC00954, MATN3, TTC32, WDR35
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206079
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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