A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354296



Internal ID21011849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:37906601..37993200hg38UCSC Ensembl
chr2:38133744..38220343hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg3886600
hg1986600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3836n223
Supporting Variantsnssv18206913
Samples
Known GenesRMDN2, RMDN2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354296
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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