A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5554708



Internal ID327886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97733547..97745469hg38UCSC Ensembl
chr10:99493304..99505226hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3811923
hg1911923
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17039785
Samples
Known GenesZFYVE27
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5554708
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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