A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562850



Internal ID20935921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95782704..95783361hg38UCSC Ensembl
chr5:95118408..95119065hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38658
hg19658
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5819n223
Supporting Variantsnssv18267743
Samples
Known GenesRHOBTB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562850
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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