A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4753630



Internal ID20529490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97571546..97571546hg38UCSC Ensembl
chr13:98223800..98223800hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16262779
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4753630
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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