A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072496



Internal ID21438755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110648194..110648253hg38UCSC Ensembl
chr11:110518917..110518976hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5589423
Supporting Variants
SamplesHG00732
Known GenesARHGAP20
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072496
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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