A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465753



Internal ID21123306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:100951295..100951747hg38UCSC Ensembl
chr11:100822026..100822478hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38453
hg19453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985532
Samples
Known GenesARHGAP42
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465753
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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