A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6348050



Internal ID21005603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:225866376..226093605hg38UCSC Ensembl
chr2:226731092..226958321hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg38227230
hg19227230
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084154
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6348050
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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