A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571412



Internal ID20944483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:64502785..64509199hg38UCSC Ensembl
chr8:65415342..65421756hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg386415
hg196415
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278440
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571412
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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