A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943013



Internal ID22718457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46932704..46932760hg38UCSC Ensembl
chr19:47435961..47436017hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402620
Samples
Known GenesARHGAP35
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943013
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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