A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269815



Internal ID20836855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107326173..107326704hg38UCSC Ensembl
chr6:107647377..107647908hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38532
hg19532
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563118
Supporting Variants
Samples
Known GenesPDSS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269815
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00041


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