A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337906



Internal ID20995459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:105588803..105592180hg38UCSC Ensembl
chr2:106205260..106208637hg19UCSC Ensembl
Cytoband2q12.2
Allele length
AssemblyAllele length
hg383378
hg193378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18076640
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337906
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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