A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552580



Internal ID20925705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45442857..45443563hg38UCSC Ensembl
chr1:45908529..45909235hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38707
hg19707
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251086
Samples
Known GenesTESK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552580
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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