A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4390614



Internal ID21381749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39454333..39454654hg38UCSC Ensembl
chr13:40028470..40028791hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15705552
Samples
Known GenesLHFP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4390614
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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