A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569027



Internal ID20942098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107918712..107918958hg38UCSC Ensembl
chr6:108239916..108240162hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38247
hg19247
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269225
Samples
Known GenesSEC63
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569027
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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