A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763924



Internal ID20539784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90570668..90570668hg38UCSC Ensembl
chr13:91222922..91222922hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272111
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763924
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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