A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443714



Internal ID21101267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:25405704..25509238hg38UCSC Ensembl
chr11:25427250..25530784hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38103535
hg19103535
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189987
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443714
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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