A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564169



Internal ID20937240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15114961..15116438hg38UCSC Ensembl
chr6:15115192..15116669hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg381478
hg191478
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6062n223
Supporting Variantsnssv18269358
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564169
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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