A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5591723



Internal ID21540301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19642665..19642979hg38UCSC Ensembl
chr9:19642663..19642977hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17161039
SamplesNA19238
Known GenesSLC24A2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5591723
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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