A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564711



Internal ID20937782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:50034982..50038536hg38UCSC Ensembl
chr6:50002695..50006249hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg383555
hg193555
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272046
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564711
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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