A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5587023



Internal ID21535581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39481631..39481690hg38UCSC Ensembl
chr17:37637884..37637943hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096817
SamplesHG00732
Known GenesCDK12
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5587023
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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