A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470688



Internal ID21128241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:100869575..100870207hg38UCSC Ensembl
chr11:100740306..100740938hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38633
hg19633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985118
Samples
Known GenesARHGAP42
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470688
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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