A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559947



Internal ID20933018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:131994068..131995011hg38UCSC Ensembl
chr6:132315208..132316151hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38944
hg19944
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6405n223
Supporting Variantsnssv18271886
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559947
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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