A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18273328



Internal ID20840368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63539118..63539653hg38UCSC Ensembl
chr6:64249023..64249558hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565943
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18273328
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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