A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553568



Internal ID20926678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:201960371..201960428hg38UCSC Ensembl
chr1:201929499..201929556hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248890
Samples
Known GenesTIMM17A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553568
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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