A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457888



Internal ID21115441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:91143533..91360489hg38UCSC Ensembl
chr11:90876701..91093656hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38216957
hg19216956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995133
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457888
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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