A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290238



Internal ID20499456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39454338..39454661hg38UCSC Ensembl
chr13:40028475..40028798hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735757
Supporting Variants
Samples
Known GenesLHFP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290238
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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