A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557089



Internal ID20930160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:151164646..151165171hg38UCSC Ensembl
chr4:152085798..152086323hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38526
hg19526
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263836
Samples
Known GenesSH3D19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557089
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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