A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562606



Internal ID20935677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:57270723..57683643hg38UCSC Ensembl
chr6:57135521..57542463hg19UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg38412921
hg19406943
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270991
Samples
Known GenesPRIM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562606
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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