A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558491



Internal ID20931562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:63196418..63198499hg38UCSC Ensembl
chr8:64108976..64111057hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg382082
hg192082
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278420
Samples
Known GenesYTHDF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558491
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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