A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16259709



Internal ID20468927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:26999275..26999366hg38UCSC Ensembl
chr17:25326301..25326392hg19UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735008
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16259709
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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