A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551225



Internal ID20924362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27796910..27798297hg38UCSC Ensembl
chr1:28123421..28124808hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg381388
hg191388
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249044
Samples
Known GenesSTX12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551225
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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