A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450788



Internal ID21108341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103390506..103461933hg38UCSC Ensembl
chr10:105150263..105221690hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg3871428
hg1971428
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181083
Samples
Known GenesCALHM1, CALHM2, MIR1307, PDCD11, USMG5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450788
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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