A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5475368



Internal ID253006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13844412..13844482hg38UCSC Ensembl
chr10:13886412..13886482hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17030308
Samples
Known GenesFRMD4A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5475368
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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