A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181083



Internal ID20748123
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 StatusS
Merged Variantsnsv6450788
Supporting Variants
Samples
Known GenesCALHM1, CALHM2, MIR1307, PDCD11, USMG5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181083
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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