A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745963



Internal ID20521974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39481621..39481698hg38UCSC Ensembl
chr17:37637874..37637951hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264599
Samples
Known GenesCDK12
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745963
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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