A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735757



Internal ID20511700
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 StatusM
Merged Variants
Supporting Variantsnssv16290238
Samples
Known GenesLHFP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735757
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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