A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18273181



Internal ID20840221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144578134..144578496hg38UCSC Ensembl
chr6:144899270..144899632hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38363
hg19363
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566068
Supporting Variants
Samples
Known GenesUTRN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18273181
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00049


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