A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5654655



Internal ID21602960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62436733..62436733hg38UCSC Ensembl
chr17:60514094..60514094hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17095065
SamplesHG03732
Known GenesMETTL2A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5654655
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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