A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468082



Internal ID21125635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58748784..58749449hg38UCSC Ensembl
chr11:58516257..58516922hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38666
hg19666
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991960
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468082
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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