A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184048



Internal ID20751088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:47928601..47961300hg38UCSC Ensembl
chr10:47093736..47126394hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3832700
hg1932659
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443475
Supporting Variants
Samples
Known GenesLINC00842
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184048
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0178


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