A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183167



Internal ID20750207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113161554..113163273hg38UCSC Ensembl
chr10:114921313..114923032hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg381720
hg191720
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6455270
Supporting Variants
Samples
Known GenesTCF7L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183167
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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