A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465250



Internal ID21122803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:88348133..88353796hg38UCSC Ensembl
chr11:88081301..88086964hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg385664
hg195664
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995036
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465250
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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