A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733774



Internal ID20509704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99476902..99477004hg38UCSC Ensembl
chr13:100129156..100129258hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289830
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733774
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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