A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484387



Internal ID261798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73417850..73418164hg38UCSC Ensembl
chr10:75177608..75177922hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17036960
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484387
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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