A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093942



Internal ID22003175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101976000..101976000hg38UCSC Ensembl
chr10:103735757..103735757hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17591276
Samples
Known GenesC10orf76
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093942
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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