A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209777



Internal ID20776818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:43710197..43820896hg38UCSC Ensembl
chr2:43937336..44048035hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38110700
hg19110700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6346399
Supporting Variants
Samples
Known GenesABCG5, DYNC2LI1, PLEKHH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209777
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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