A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460575



Internal ID21118128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56946589..56956949hg38UCSC Ensembl
chr11:56714064..56724424hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3810361
hg1910361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993403
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460575
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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