A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473532



Internal ID21131085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107405401..107406200hg38UCSC Ensembl
chr11:107276127..107276926hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986537
Samples
Known GenesCWF19L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473532
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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