A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5498127



Internal ID275132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119935872..119937288hg38UCSC Ensembl
chr10:121695384..121696800hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg381417
hg191417
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17039367
Samples
Known GenesSEC23IP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5498127
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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