A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104923



Internal ID22014157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113411927..113412250hg38UCSC Ensembl
chr10:115171686..115172009hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583516
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104923
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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