A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463539



Internal ID21121092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95588556..95589030hg38UCSC Ensembl
chr11:95321720..95322194hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38475
hg19475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995580
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463539
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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