A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459574



Internal ID21117127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:37746901..37808100hg38UCSC Ensembl
chr11:37768451..37829650hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3861200
hg1961200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1024n223
Supporting Variantsnssv18191484
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459574
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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