A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336121



Internal ID20993674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:223672816..223674306hg38UCSC Ensembl
chr2:224537533..224539023hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg381491
hg191491
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206266
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336121
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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