A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743187



Internal ID20519174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113600655..113600744hg38UCSC Ensembl
chr13:114254970..114255059hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16281279
Samples
Known GenesTFDP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743187
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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