A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189042



Internal ID20756082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103392774..103551394hg38UCSC Ensembl
chr10:105152531..105311151hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg38158621
hg19158621
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440427
Supporting Variants
Samples
Known GenesCALHM1, CALHM2, CALHM3, MIR1307, NEURL1, PDCD11, USMG5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189042
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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