A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5481299



Internal ID258786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95949200..96035000hg38UCSC Ensembl
chr10:97708957..97794757hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3885801
hg1985801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038775
Samples
Known GenesCC2D2B, ENTPD1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5481299
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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