A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5511779



Internal ID288349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121352384..121359851hg38UCSC Ensembl
chr10:123111898..123119365hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg387468
hg197468
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17037842
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5511779
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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