A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5511646



Internal ID288219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113053838..113053920hg38UCSC Ensembl
chr10:114813597..114813679hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17039117
Samples
Known GenesTCF7L2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5511646
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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