A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5480185



Internal ID257695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100360359..100360542hg38UCSC Ensembl
chr10:102120116..102120299hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038464
Samples
Known GenesSCD
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5480185
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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