A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269895



Internal ID20836935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162156712..162706109hg38UCSC Ensembl
chr6:162577744..163127141hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38549398
hg19549398
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570388
Supporting Variants
Samples
Known GenesPARK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269895
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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