A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5476203



Internal ID253819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45838765..45958265hg38UCSC Ensembl
chr10:46334213..46426964hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38119501
hg1992752
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17034497
Samples
Known GenesAGAP4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5476203
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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