A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909484



Internal ID22684694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96525750..96525801hg38UCSC Ensembl
chr10:98285507..98285558hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360388
Samples
Known GenesTM9SF3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909484
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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