A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17472141



Internal ID22530033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57693819..57705354hg38UCSC Ensembl
chr16:57727731..57739266hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3811536
hg1911536
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5875312
Supporting Variants
Samples
Known GenesCCDC135
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17472141
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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