A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17364312



Internal ID22589981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24634312..24635034hg38UCSC Ensembl
chr10:24923241..24923963hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38723
hg19723
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5927205
Supporting Variants
Samples
Known GenesARHGAP21
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17364312
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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