A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029598



Internal ID21938941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86025623..86025688hg38UCSC Ensembl
chr11:85736665..85736730hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596240
Samples
Known GenesPICALM
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029598
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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