A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5500037



Internal ID276986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:108777974..108779218hg38UCSC Ensembl
chr10:110537732..110538976hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg381245
hg191245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17039593
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5500037
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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