A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267894



Internal ID20477112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57680049..57680108hg38UCSC Ensembl
chr16:57713961..57714020hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736592
Supporting Variants
Samples
Known GenesGPR97
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267894
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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