A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562639



Internal ID20935710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:65611919..65612582hg38UCSC Ensembl
chr8:66524154..66524817hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38664
hg19664
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278453
Samples
Known GenesARMC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562639
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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