A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462859



Internal ID21120412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93917703..94047376hg38UCSC Ensembl
chr11:93650869..93780542hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38129674
hg19129674
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995253
Samples
Known GenesHEPHL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462859
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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