A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039115



Internal ID93818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112991440..112991494hg38UCSC Ensembl
chr10:114751199..114751253hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6143179
Supporting Variants
Samples
Known GenesTCF7L2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039115
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.030876


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