A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566438



Internal ID20939509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134300444..134300910hg38UCSC Ensembl
chr6:134621582..134622048hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38467
hg19467
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6411n223
Supporting Variantsnssv18271932
Samples
Known GenesSGK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566438
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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