A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17618437



Internal ID21810484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57680108..57680218hg38UCSC Ensembl
chr16:57714020..57714130hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6026152
Supporting Variants
Samples
Known GenesGPR97
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17618437
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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