A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541397



Internal ID20914678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:51398088..51399403hg38UCSC Ensembl
chr1:51863760..51865075hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg381316
hg191316
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251660
Samples
Known GenesEPS15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541397
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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