A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978154



Internal ID20545194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113001470..113001917hg38UCSC Ensembl
chr10:114761229..114761676hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38448
hg19448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437245
Supporting Variants
Samples
Known GenesTCF7L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978154
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00047


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