A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556264



Internal ID20929335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:147677133..147677453hg38UCSC Ensembl
chr4:148598284..148598604hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264810
Samples
Known GenesPRMT10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556264
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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