A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16277813



Internal ID20487031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:34838342..34838481hg38UCSC Ensembl
chr17:33165361..33165500hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749366
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16277813
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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