A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025722



Internal ID21935065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65970430..65970491hg38UCSC Ensembl
chr17:63966548..63966609hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626931
Samples
Known GenesCEP112
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025722
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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