A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567822



Internal ID20940893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99704435..99704916hg38UCSC Ensembl
chr7:99302058..99302539hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38482
hg19482
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275866
Samples
Known GenesCYP3A7-CYP3AP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567822
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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