A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445078



Internal ID21102631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112346501..112379600hg38UCSC Ensembl
chr10:114106259..114139358hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3833100
hg1933100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185236
Samples
Known GenesACSL5, GUCY2GP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445078
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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