A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16291386



Internal ID20500604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39902653..39903045hg38UCSC Ensembl
chr17:38058906..38059298hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38393
hg19393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4744871
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16291386
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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