A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560027



Internal ID20933098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:122739451..122740120hg38UCSC Ensembl
chr6:123060596..123061265hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38670
hg19670
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271129
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560027
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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