A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566519



Internal ID20939590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109270727..109271368hg38UCSC Ensembl
chr6:109591930..109592571hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38642
hg19642
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6361n223
Supporting Variantsnssv18267811
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566519
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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