A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489751



Internal ID267022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:27707044..27707273hg38UCSC Ensembl
chr10:27995973..27996202hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38230
hg19230
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17033334
Samples
Known GenesMKX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489751
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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