A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17472258



Internal ID22530150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66487193..66488792hg38UCSC Ensembl
chr16:66521096..66522695hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5870412
Supporting Variants
Samples
Known GenesBEAN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17472258
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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