A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924432



Internal ID22699659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:100805737..100806962hg38UCSC Ensembl
chr11:100676468..100677693hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg381226
hg191226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361988
Samples
Known GenesARHGAP42
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924432
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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