A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565260



Internal ID20938331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42186474..42187162hg38UCSC Ensembl
chr6:42154212..42154900hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38689
hg19689
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271281
Samples
Known GenesGUCA1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565260
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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