A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271939



Internal ID20838979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134417961..134418246hg38UCSC Ensembl
chr6:134739099..134739384hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38286
hg19286
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567474
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271939
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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