A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345105



Internal ID21002658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:20493161..20503804hg38UCSC Ensembl
chr2:20692921..20703564hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3810644
hg1910644
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082306
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345105
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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