A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562696



Internal ID20935767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26641854..26654701hg38UCSC Ensembl
chr4:26643476..26656323hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3812848
hg1912848
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264987
Samples
Known GenesTBC1D19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562696
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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