A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249069



Internal ID20816109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28062730..28063391hg38UCSC Ensembl
chr1:28389241..28389902hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38662
hg19662
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547067
Supporting Variants
Samples
Known GenesEYA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249069
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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