A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760902



Internal ID20536762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110201264..110201264hg38UCSC Ensembl
chr13:110853611..110853611hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294823
Samples
Known GenesCOL4A1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760902
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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