A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272378



Internal ID20839418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13607794..13608386hg38UCSC Ensembl
chr6:13608026..13608618hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38593
hg19593
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573803
Supporting Variants
Samples
Known GenesSIRT5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272378
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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