A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16953524



Internal ID36367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:105571362..105571517hg38UCSC Ensembl
chr4:106492519..106492674hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5473353
Supporting Variants
Samples
Known GenesARHGEF38
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16953524
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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