A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466795



Internal ID21124348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:97704826..97785274hg38UCSC Ensembl
chr11:97575826..97656274hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3880449
hg1980449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995826
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466795
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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