A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5469002



Internal ID246795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:105656691..105661966hg38UCSC Ensembl
chr4:106577848..106583123hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg385276
hg195276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16954463
Samples
Known GenesARHGEF38
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5469002
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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