A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272978



Internal ID20482196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75162721..75162907hg38UCSC Ensembl
chr17:73158816..73159002hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747390
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272978
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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