A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274854



Internal ID20841894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87379829..87380756hg38UCSC Ensembl
chr6:88089547..88090474hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38928
hg19928
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571610
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274854
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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