A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343678



Internal ID21001231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:203312975..203317856hg38UCSC Ensembl
chr2:204177698..204182579hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg384882
hg194882
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084378
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343678
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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