A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17628846



Internal ID21820893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57883571..57883664hg38UCSC Ensembl
chr17:55960932..55961025hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6027717
Supporting Variants
Samples
Known GenesCUEDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17628846
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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