A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535889



Internal ID20909242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27780963..27781122hg38UCSC Ensembl
chr1:28107474..28107633hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249043
Samples
Known GenesSTX12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535889
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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