A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565318



Internal ID20938389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150572855..150573317hg38UCSC Ensembl
chr3:150290642..150291104hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38463
hg19463
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263201
Samples
Known GenesEIF2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565318
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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