A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16285091



Internal ID20494309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78760381..78760509hg38UCSC Ensembl
chr17:76756463..76756591hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747380
Supporting Variants
Samples
Known GenesCYTH1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16285091
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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