A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269814



Internal ID20836854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107310068..107310940hg38UCSC Ensembl
chr6:107631272..107632144hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38873
hg19873
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564995
Supporting Variants
Samples
Known GenesPDSS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269814
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0002


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