A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17585021



Internal ID21777064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:65662661..65662661hg38UCSC Ensembl
chr8:66574896..66574896hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6070580
Supporting Variants
Samples
Known GenesMTFR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17585021
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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