A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5500500



Internal ID277433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103220385..103223994hg38UCSC Ensembl
chr10:104980142..104983751hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg383610
hg193610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17040001
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5500500
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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