A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271189



Internal ID20838229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:127373693..127374744hg38UCSC Ensembl
chr6:127694838..127695889hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg381052
hg191052
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6569279
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271189
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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