A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563812



Internal ID20936883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:52458444..52459288hg38UCSC Ensembl
chr4:53324610..53325454hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38845
hg19845
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266393
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563812
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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