A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027717



Internal ID21937060
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 StatusM
Merged Variants
Supporting Variantsnssv17628846
Samples
Known GenesCUEDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027717
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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