A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341317



Internal ID20998870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:220582478..220583243hg38UCSC Ensembl
chr2:221447199..221447964hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38766
hg19766
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18086184
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341317
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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