A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469861



Internal ID21127414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35007225..35028495hg38UCSC Ensembl
chr11:35028772..35050042hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3821271
hg1921271
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196229
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469861
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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