A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341286



Internal ID20998839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:231634330..231643734hg38UCSC Ensembl
chr2:232499041..232508445hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg389405
hg199405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18086589
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341286
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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