A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186399



Internal ID20753439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:117015577..117024604hg38UCSC Ensembl
chr10:118775088..118784115hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg389028
hg199028
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450626
Supporting Variants
Samples
Known GenesKIAA1598
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186399
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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