A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545144



Internal ID20918376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:69282927..69283373hg38UCSC Ensembl
chr3:69332078..69332524hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38447
hg19447
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262863
Samples
Known GenesFRMD4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545144
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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