A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269806



Internal ID20836846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107239186..107239883hg38UCSC Ensembl
chr6:107560390..107561087hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38698
hg19698
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571006
Supporting Variants
Samples
Known GenesPDSS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269806
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00024


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