A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267785



Internal ID20834825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108314017..108314609hg38UCSC Ensembl
chr6:108635221..108635813hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38593
hg19593
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563072
Supporting Variants
Samples
Known GenesLACE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267785
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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