A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539741



Internal ID20913036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:212743303..212745105hg38UCSC Ensembl
chr1:212916645..212918447hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg381803
hg191803
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248521
Samples
Known GenesNSL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539741
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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