A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438775



Internal ID21096328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18869501..18883400hg38UCSC Ensembl
chr11:18891048..18904947hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3813900
hg1913900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988682
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438775
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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