A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337198



Internal ID20994751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:37923201..37937700hg38UCSC Ensembl
chr2:38150344..38164843hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg3814500
hg1914500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3837n223
Supporting Variantsnssv18206918
Samples
Known GenesRMDN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337198
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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