A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18096129



Internal ID20663169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154033847..154253028hg38UCSC Ensembl
chr3:153751636..153970817hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38219182
hg19219182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357631
Supporting Variants
Samples
Known GenesARHGEF26, ARHGEF26-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18096129
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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