A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17082644



Internal ID21407016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69491108..69491108hg38UCSC Ensembl
chr17:67487249..67487249hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5653070
Supporting Variants
SamplesHG00512
Known GenesMAP2K6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17082644
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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