A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651477



Internal ID21599782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78175213..78175213hg38UCSC Ensembl
chr17:76171294..76171294hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38538
hg19538
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17084857
SamplesHG00732
Known GenesTK1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651477
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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