A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352042



Internal ID21009595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:185268901..185843800hg38UCSC Ensembl
chr2:186133628..186708527hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38574900
hg19574900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205361
Samples
Known GenesFSIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352042
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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