A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565898



Internal ID20938969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:86167776..86180297hg38UCSC Ensembl
chr7:85797092..85809613hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3812522
hg1912522
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276813
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565898
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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