A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455882



Internal ID21113435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:88502476..88503626hg38UCSC Ensembl
chr11:88235644..88236794hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg381151
hg191151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995052
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455882
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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