A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747564



Internal ID20523583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67967273..67967358hg38UCSC Ensembl
chr17:65963389..65963474hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261989
Samples
Known GenesBPTF
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747564
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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