A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865999



Internal ID22640934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:132561021..132570100hg38UCSC Ensembl
chr8:133573268..133582348hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg389080
hg199081
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506893
Samples
Known GenesHPYR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865999
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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