A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183318



Internal ID20750358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1143149..1249515hg38UCSC Ensembl
chr10:1189089..1291567hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38106367
hg19102479
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445353
Supporting Variants
Samples
Known GenesADARB2, LINC00200
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183318
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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