A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451639



Internal ID21109192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118621998..118692736hg38UCSC Ensembl
chr10:120381510..120452248hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3870739
hg1970739
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194248
Samples
Known GenesCACUL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451639
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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