A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351947



Internal ID21009500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:37921601..37939000hg38UCSC Ensembl
chr2:38148744..38166143hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg3817400
hg1917400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3837n223
Supporting Variantsnssv18206916
Samples
Known GenesRMDN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351947
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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