A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436641



Internal ID21094194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42093470..42166360hg38UCSC Ensembl
chr10:42596688..42661808hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3872891
hg1965121
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178597
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436641
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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