A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462885



Internal ID21120438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93754832..93765974hg38UCSC Ensembl
chr11:93487998..93499140hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3811143
hg1911143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995248
Samples
Known GenesC11orf54
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462885
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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