A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5506929



Internal ID283661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125008360..125008652hg38UCSC Ensembl
chr10:126696929..126697221hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038895
Samples
Known GenesCTBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5506929
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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