A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559887



Internal ID20932958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24772853..24773519hg38UCSC Ensembl
chr6:24773081..24773747hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38667
hg19667
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270871
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559887
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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