A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4392166



Internal ID21383196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149327061..149327300hg38UCSC Ensembl
chr5:148706624..148706863hg19UCSC 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 Variantsnssv15703620
Samples
Known GenesAFAP1L1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4392166
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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