A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470005



Internal ID21127558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67266838..67272455hg38UCSC Ensembl
chr11:67034309..67039926hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg385618
hg195618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993481
Samples
Known GenesADRBK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470005
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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