A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561100



Internal ID20934171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121802366..121802421hg38UCSC Ensembl
chr4:122723521..122723576hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263640
Samples
Known GenesEXOSC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561100
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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