A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462613



Internal ID21120166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92141023..92159617hg38UCSC Ensembl
chr11:91874189..91892783hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3818595
hg1918595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995353
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462613
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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