A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489157



Internal ID266446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72590408..72591222hg38UCSC Ensembl
chr10:74350166..74350980hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38815
hg19815
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17037542
Samples
Known GenesMICU1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489157
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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