A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561065



Internal ID20934136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:47515053..47516193hg38UCSC Ensembl
chr4:47517070..47518210hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg381141
hg191141
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266348
Samples
Known GenesATP10D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561065
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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