A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564843



Internal ID20937914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3884957..3887218hg38UCSC Ensembl
chr6:3885191..3887452hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg382262
hg192262
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271401
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564843
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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