A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249059



Internal ID20816099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27976328..27977005hg38UCSC Ensembl
chr1:28302839..28303516hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38678
hg19678
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536922
Supporting Variants
Samples
Known GenesEYA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249059
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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