A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564864



Internal ID20937935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30594083..30594786hg38UCSC Ensembl
chr8:30451600..30452303hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38704
hg19704
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277695
Samples
Known GenesGTF2E2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564864
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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