A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16278995



Internal ID20488213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:77150471..77314506hg38UCSC Ensembl
chr16:77184368..77348403hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38164036
hg19164036
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4754371
Supporting Variants
Samples
Known GenesADAMTS18, MON1B, SYCE1L
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16278995
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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