A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561606



Internal ID20934677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38059016..38060740hg38UCSC Ensembl
chr8:37916534..37918258hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg381725
hg191725
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277893
Samples
Known GenesEIF4EBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561606
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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