A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274842



Internal ID20841882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:8660035..9108021hg38UCSC Ensembl
chr6:8660268..9108254hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38447987
hg19447987
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567145
Supporting Variants
Samples
Known GenesLOC100506207
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274842
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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