A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944451



Internal ID22719916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46928697..46934160hg38UCSC Ensembl
chr19:47431954..47437417hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg385464
hg195464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17406760
Samples
Known GenesARHGAP35
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944451
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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