A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572298



Internal ID20945369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112990266..112991726hg38UCSC Ensembl
chr6:113311468..113312928hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381461
hg191461
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268525
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572298
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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