A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569448



Internal ID20942519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:27369532..27371311hg38UCSC Ensembl
chr8:27227049..27228828hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg381780
hg191780
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277582
Samples
Known GenesPTK2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569448
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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