A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467329



Internal ID21124882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63318501..63336400hg38UCSC Ensembl
chr11:63085973..63103872hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3817900
hg1917900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993782
Samples
Known GenesMIR3680-1, MIR3680-2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467329
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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