A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5478073



Internal ID255637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100308309..100308385hg38UCSC Ensembl
chr9:103070591..103070667hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024995
Samples
Known GenesTEX10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5478073
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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