A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099711



Internal ID22008944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104036045..104036045hg38UCSC Ensembl
chr10:105795803..105795803hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583152
Samples
Known GenesCOL17A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099711
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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