A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335669



Internal ID20993222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:224683875..224707541hg38UCSC Ensembl
chr2:225548592..225572258hg19UCSC Ensembl
Cytoband2q36.2
Allele length
AssemblyAllele length
hg3823667
hg1923667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18083817
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335669
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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