A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292459



Internal ID20501677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45051740..45051892hg38UCSC Ensembl
chr17:43129108..43129260hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733975
Supporting Variants
Samples
Known GenesDCAKD
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292459
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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