A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875312



Internal ID22650269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57693819..57705354hg38UCSC Ensembl
chr16:57727731..57739266hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3811536
hg1911536
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472141
Samples
Known GenesCCDC135
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875312
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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