A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865484



Internal ID22640419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:100805776..100809349hg38UCSC Ensembl
chr11:100676507..100680080hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg383574
hg193574
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463158
Samples
Known GenesARHGAP42
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865484
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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