A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462565



Internal ID21120118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:87480818..87481445hg38UCSC Ensembl
chr11:87191860..87192487hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38628
hg19628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994948
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462565
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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