A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566178



Internal ID20939249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138789590..138790403hg38UCSC Ensembl
chr6:139110727..139111540hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38814
hg19814
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272473
Samples
Known GenesCCDC28A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566178
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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