A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468733



Internal ID21126286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123289270..123310634hg38UCSC Ensembl
chr11:123159978..123181342hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3821365
hg1921365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987672
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468733
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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