A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5532977



Internal ID308876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89286108..89287123hg38UCSC Ensembl
chr15:89829339..89830354hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381016
hg191016
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704106
Samples
Known GenesFANCI
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5532977
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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