A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554395



Internal ID20927491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:179891476..179892194hg38UCSC Ensembl
chr1:179860611..179861329hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38719
hg19719
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248838
Samples
Known GenesTOR1AIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554395
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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