A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863795



Internal ID22638730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129037245..129038844hg38UCSC Ensembl
chr11:128907140..128908739hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465078
Samples
Known GenesARHGAP32
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863795
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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