A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5551645



Internal ID325081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96009540..96009578hg38UCSC Ensembl
chr10:97769297..97769335hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038779
Samples
Known GenesCC2D2B, ENTPD1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5551645
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer