A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448470



Internal ID21106023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102441225..102487982hg38UCSC Ensembl
chr10:104200982..104247739hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3846758
hg1946758
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185070
Samples
Known GenesACTR1A, C10orf95, LOC100505761, TMEM180
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448470
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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