A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100340



Internal ID22009573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103583767..103583767hg38UCSC Ensembl
chr10:105343524..105343524hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg38251
hg19251
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580173
Samples
Known GenesNEURL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100340
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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