A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457336



Internal ID21114889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:37745701..37806000hg38UCSC Ensembl
chr11:37767251..37827550hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3860300
hg1960300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1024n223
Supporting Variantsnssv18186158
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457336
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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