A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451453



Internal ID21109006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112974728..112980836hg38UCSC Ensembl
chr10:114734487..114740595hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg386109
hg196109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978153
Samples
Known GenesTCF7L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451453
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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