A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18270141



Internal ID20837181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1990084..1990572hg38UCSC Ensembl
chr6:1990318..1990806hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38489
hg19489
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571786
Supporting Variants
Samples
Known GenesGMDS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18270141
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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