A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5550205



Internal ID323789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114215151..114215181hg38UCSC Ensembl
chr10:115974910..115974940hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17039197
Samples
Known GenesTDRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5550205
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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