A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4768226



Internal ID20544086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63559341..63559341hg38UCSC Ensembl
chr17:61636702..61636702hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280363
Samples
Known GenesDCAF7
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4768226
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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