A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548214



Internal ID20921410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:179874748..179874983hg38UCSC Ensembl
chr1:179843883..179844118hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248836
Samples
Known GenesTOR1AIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548214
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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