A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572688



Internal ID20945759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:45093391..45102166hg38UCSC Ensembl
chr6:45061128..45069903hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg388776
hg198776
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271386
Samples
Known GenesSUPT3H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572688
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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