A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559272



Internal ID20932343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:47454828..47455089hg38UCSC Ensembl
chr4:47456845..47457106hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38262
hg19262
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266344
Samples
Known GenesCOMMD8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559272
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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