A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440586



Internal ID21098139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110224601..110226200hg38UCSC Ensembl
chr10:111984359..111985958hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187278
Samples
Known GenesMXI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440586
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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