A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181017



Internal ID20748057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5561496..5613774hg38UCSC Ensembl
chr10:5603459..5655737hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3852279
hg1952279
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440120
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181017
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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