A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540366



Internal ID20913657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:49709507..49715857hg38UCSC Ensembl
chr1:50175179..50181529hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg386351
hg196351
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251185
Samples
Known GenesAGBL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540366
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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