A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13701290



Internal ID21223124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24656663..24656760hg38UCSC Ensembl
chr10:24945592..24945689hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2788867
Supporting Variants
Samples
Known GenesARHGAP21
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13701290
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.25


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