A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751283



Internal ID20527144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:29908967..29908967hg38UCSC Ensembl
chr13:30483104..30483104hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286964
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751283
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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