A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595127



Internal ID20968198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:21615240..21616343hg38UCSC Ensembl
chr18:19195201..19196304hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg381104
hg191104
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244146
Samples
Known GenesSNRPD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595127
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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