A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547675



Internal ID20920876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:179908872..179909398hg38UCSC Ensembl
chr1:179878007..179878533hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38527
hg19527
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248841
Samples
Known GenesTOR1AIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547675
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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