A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347890



Internal ID21005443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:186325854..186345998hg38UCSC Ensembl
chr2:187190581..187210725hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3820145
hg1920145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080095
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347890
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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