A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569980



Internal ID20943051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25316451..25323656hg38UCSC Ensembl
chr6:25316679..25323884hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg387206
hg197206
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270892
Samples
Known GenesLRRC16A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569980
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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