A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452411



Internal ID21109964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112341901..112356400hg38UCSC Ensembl
chr10:114101659..114116158hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3814500
hg1914500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181861
Samples
Known GenesGUCY2GP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452411
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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