A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354427



Internal ID21011980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:196586001..196597900hg38UCSC Ensembl
chr2:197450725..197462624hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3811900
hg1911900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208241
Samples
Known GenesHECW2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354427
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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