A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5493893



Internal ID271057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32928154..32929820hg38UCSC Ensembl
chr10:33217082..33218748hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg381667
hg191667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17032975
Samples
Known GenesITGB1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5493893
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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