A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5509048



Internal ID285717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122791194..122797323hg38UCSC Ensembl
chr10:124550710..124556839hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg386130
hg196130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038830
Samples
Known GenesFLJ46361
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5509048
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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