A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536854



Internal ID20910198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:5099191..5100061hg38UCSC Ensembl
chr3:5140876..5141746hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38871
hg19871
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260766
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536854
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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