A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588957



Internal ID20962028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62160032..62160549hg38UCSC Ensembl
chr18:59827265..59827782hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38518
hg19518
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245429
Samples
Known GenesPIGN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588957
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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