A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543467



Internal ID20916715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86878565..86880381hg38UCSC Ensembl
chr1:87344248..87346064hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg381817
hg191817
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251909
Samples
Known GenesSEP15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543467
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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