A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564492



Internal ID20937563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:103992122..103993079hg38UCSC Ensembl
chr8:105004350..105005307hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38958
hg19958
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7444n223
Supporting Variantsnssv18276316
Samples
Known GenesRIMS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564492
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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