A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577204



Internal ID20950275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:45738747..45739956hg38UCSC Ensembl
chr18:43318712..43319921hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg381210
hg191210
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246867
Samples
Known GenesSLC14A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577204
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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