A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455236



Internal ID21112789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87836265..87847187hg38UCSC Ensembl
chr10:89596022..89606944hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3810923
hg1910923
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191034
Samples
Known GenesCFL1P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455236
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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