A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562706



Internal ID20935777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169742839..169743351hg38UCSC Ensembl
chr4:170663990..170664502hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38513
hg19513
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264394
Samples
Known GenesC4orf27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562706
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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