A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551966



Internal ID20925097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28052864..28055463hg38UCSC Ensembl
chr1:28379375..28381974hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249068
Samples
Known GenesEYA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551966
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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