A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559616



Internal ID20932687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92103532..92104219hg38UCSC Ensembl
chr7:91732846..91733533hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg38688
hg19688
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276905
Samples
Known GenesAKAP9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559616
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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