A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850637



Internal ID22625572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:43081704..43105846hg38UCSC Ensembl
chr8:42936847..42960989hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3824143
hg1924143
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509222, nssv17506670
Samples
Known GenesFNTA, POMK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850637
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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