A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458598



Internal ID21116151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93520180..93529099hg38UCSC Ensembl
chr11:93253346..93262265hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg388920
hg198920
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995232
Samples
Known GenesSMCO4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458598
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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