A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584033



Internal ID21532566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149327060..149327299hg38UCSC Ensembl
chr5:148706623..148706862hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38240
hg19240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17122645
SamplesNA24385
Known GenesAFAP1L1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584033
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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