A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474854



Internal ID21132407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:121212371..121213004hg38UCSC Ensembl
chr11:121083080..121083713hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38634
hg19634
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987008
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474854
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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