A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5509372



Internal ID286026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:107689638..107691087hg38UCSC Ensembl
chr10:109449396..109450845hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg381450
hg191450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17041010
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5509372
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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