A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573981



Internal ID20947052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:108679353..108680165hg38UCSC Ensembl
chr4:109600509..109601321hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38813
hg19813
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262965
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573981
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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