A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875401



Internal ID22650358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66559973..66569103hg38UCSC Ensembl
chr16:66593876..66603006hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg389131
hg199131
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472262
Samples
Known GenesCKLF, CKLF-CMTM1, CMTM1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875401
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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