A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585293



Internal ID20958364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63817377..68462605hg38UCSC Ensembl
chr18:61484611..66129842hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg384645229
hg194645232
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245483
Samples
Known GenesCDH19, CDH7, DSEL, HMSD, LINC00305, LOC284294, LOC400654, LOC643542, MIR5011, SERPINB10, SERPINB2, SERPINB8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585293
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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