A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861422



Internal ID22636357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:43053878..43063862hg38UCSC Ensembl
chr8:42909021..42919005hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg389985
hg199985
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509219
Samples
Known GenesFNTA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861422
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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