A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592878



Internal ID20965949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12957085..12958028hg38UCSC Ensembl
chr18:12957084..12958027hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38944
hg19944
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243465
Samples
Known GenesSEH1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592878
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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