A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550778



Internal ID20923918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19777110..19777765hg38UCSC Ensembl
chr1:20103603..20104258hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38656
hg19656
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248198
Samples
Known GenesTMCO4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550778
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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