A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556964



Internal ID20930035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:47685206..47685533hg38UCSC Ensembl
chr8:48597768..48598095hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278108
Samples
Known GenesSPIDR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556964
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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