A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560080



Internal ID20933151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160030485..160030992hg38UCSC Ensembl
chr3:159748272..159748779hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38508
hg19508
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259826
Samples
Known GenesIL12A-AS1, LINC01100
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560080
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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