A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567027



Internal ID20940098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136917677..136918531hg38UCSC Ensembl
chr6:137238815..137239669hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38855
hg19855
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272415
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567027
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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