A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757900



Internal ID20533760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39984765..39984765hg38UCSC Ensembl
chr13:40558902..40558902hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296103
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757900
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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