A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341675



Internal ID20999228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:37922001..37938900hg38UCSC Ensembl
chr2:38149144..38166043hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg3816900
hg1916900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3837n223
Supporting Variantsnssv18206917
Samples
Known GenesRMDN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341675
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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