A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449084



Internal ID21106637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100114101..100128400hg38UCSC Ensembl
chr10:101873858..101888157hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3814300
hg1914300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179712
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449084
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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