A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546305



Internal ID20919523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:96077282..96571313hg38UCSC Ensembl
chr3:95796126..96290157hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38494032
hg19494032
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262727
Samples
Known GenesMIR8060
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546305
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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