A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759680



Internal ID20535541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104036061..104036061hg38UCSC Ensembl
chr10:105795819..105795819hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg38462
hg19462
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274695
Samples
Known GenesCOL17A1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759680
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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