A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555635



Internal ID328787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85199483..85199558hg38UCSC Ensembl
chr14:85665827..85665902hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17697559
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555635
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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