A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460922



Internal ID21118475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68280620..68281678hg38UCSC Ensembl
chr11:68048088..68049146hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg381059
hg191059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993561
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460922
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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