A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272444



Internal ID20839484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138061639..138061787hg38UCSC Ensembl
chr6:138382776..138382924hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568845
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272444
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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