A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453613



Internal ID21111166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:26586701..26588100hg38UCSC Ensembl
chr11:26608248..26609647hg19UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191179
Samples
Known GenesANO3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453613
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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