A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271869



Internal ID20838909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:131306705..131307333hg38UCSC Ensembl
chr6:131627845..131628473hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38629
hg19629
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573042
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271869
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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