A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440903



Internal ID21098456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27805501..27810400hg38UCSC Ensembl
chr11:27827048..27831947hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg384900
hg194900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187029
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440903
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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