A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564802



Internal ID20937873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107073818..107074242hg38UCSC Ensembl
chr7:106714263..106714687hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38425
hg19425
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273580
Samples
Known GenesPRKAR2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564802
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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