A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541581



Internal ID20914863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:179893270..179893508hg38UCSC Ensembl
chr1:179862405..179862643hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248840
Samples
Known GenesTOR1AIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541581
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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