A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272179



Internal ID20839219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:9517558..9671029hg38UCSC Ensembl
chr6:9517791..9671262hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38153472
hg19153472
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558569
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272179
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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