A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5415550



Internal ID194807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:88000..200000hg38UCSC Ensembl
chr19:88000..200000hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38112001
hg19112001
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17720011
Samples
Known GenesLINC01002, OR4F17
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5415550
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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