A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568326



Internal ID20941397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99925189..99936027hg38UCSC Ensembl
chr7:99522812..99533650hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3810839
hg1910839
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275871
Samples
Known GenesGJC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568326
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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