A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572736



Internal ID20945807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:130918867..130919297hg38UCSC Ensembl
chr3:130637711..130638141hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38431
hg19431
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259648
Samples
Known GenesATP2C1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572736
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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