A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269358



Internal ID20836398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15114961..15116438hg38UCSC Ensembl
chr6:15115192..15116669hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg381478
hg191478
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564169
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269358
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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