A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442488



Internal ID21100041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112283087..112339233hg38UCSC Ensembl
chr10:114042845..114098991hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3856147
hg1956147
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196329
Samples
Known GenesGUCY2GP, MIR6715A, MIR6715B, TECTB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442488
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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