A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562151



Internal ID20935222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87897787..87898796hg38UCSC Ensembl
chr7:87527102..87528111hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg381010
hg191010
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276842
Samples
Known GenesDBF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562151
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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