A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567759



Internal ID20940830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15090593..15162574hg38UCSC Ensembl
chr6:15090824..15162805hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3871982
hg1971982
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269346
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567759
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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