A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5497229



Internal ID274275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:106566906..106569820hg38UCSC Ensembl
chr10:108326664..108329578hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg382915
hg192915
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17039507
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5497229
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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