A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5479554



Internal ID257073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133357265..133357508hg38UCSC Ensembl
chr9:136224141..136224384hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17030084
Samples
Known GenesSURF2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5479554
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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