A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880183



Internal ID22655153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46928533..46932883hg38UCSC Ensembl
chr19:47431790..47436140hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg384351
hg194351
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17476748
Samples
Known GenesARHGAP35
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880183
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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