A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460675



Internal ID21118228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60075015..60082849hg38UCSC Ensembl
chr11:59842488..59850322hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg387835
hg197835
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992480
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460675
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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