A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563450



Internal ID20936521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:97362886..97363278hg38UCSC Ensembl
chr6:97810762..97811154hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38393
hg19393
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272790
Samples
Known GenesMIR548H3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563450
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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