A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553169



Internal ID20926278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:224324681..224325277hg38UCSC Ensembl
chr1:224512383..224512979hg19UCSC Ensembl
Cytoband1q42.11
Allele length
AssemblyAllele length
hg38597
hg19597
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249370
Samples
Known GenesNVL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553169
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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