A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567229



Internal ID20940300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99395169..99396374hg38UCSC Ensembl
chr6:99843045..99844250hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg381206
hg191206
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272824
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567229
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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