A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767892



Internal ID20543752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77977659..77977659hg38UCSC Ensembl
chr13:78551794..78551794hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283122
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767892
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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