A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537019



Internal ID20910358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168181443..168181781hg38UCSC Ensembl
chr1:168150681..168151019hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248048
Samples
Known GenesTIPRL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537019
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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