A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460995



Internal ID21118548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63831886..63835414hg38UCSC Ensembl
chr11:63599358..63602886hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg383529
hg193529
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993817
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460995
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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