A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467077



Internal ID21124630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95337721..95340790hg38UCSC Ensembl
chr11:95070885..95073954hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg383070
hg193070
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995558
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467077
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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