A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5493852



Internal ID271017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32900471..32900726hg38UCSC Ensembl
chr10:33189399..33189654hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17032968
Samples
Known GenesITGB1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5493852
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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