A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561951



Internal ID20935022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15115017..15116544hg38UCSC Ensembl
chr6:15115248..15116775hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg381528
hg191528
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6062n223
Supporting Variantsnssv18269359
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561951
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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