A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570456



Internal ID20943527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:539147..568455hg38UCSC Ensembl
chr7:578784..608092hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3829309
hg1929309
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274622
Samples
Known GenesPRKAR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570456
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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