A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541477



Internal ID20914758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9745510..9746005hg38UCSC Ensembl
chr1:9805568..9806063hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38496
hg19496
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252783
Samples
Known GenesCLSTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541477
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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