A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209806



Internal ID20776847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:45159446..45915141hg38UCSC Ensembl
chr2:45386585..46142280hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38755696
hg19755696
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6340894
Supporting Variants
Samples
Known GenesLINC01121, PRKCE, SRBD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209806
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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