A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5487144



Internal ID264489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10298000..10303163hg38UCSC Ensembl
chr8:10155510..10160673hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg385164
hg195164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17007372
Samples
Known GenesMSRA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5487144
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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