A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5500899



Internal ID277820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:17000000..17022000hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3822001
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698878, nssv17698876
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5500899
Frequency
Sample Size3202
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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