A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353033



Internal ID21010586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:185211201..185228400hg38UCSC Ensembl
chr2:186075928..186093127hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3817200
hg1917200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4211n223
Supporting Variantsnssv18205358
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353033
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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