A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561032



Internal ID20934103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:119881492..119881947hg38UCSC Ensembl
chr8:120893732..120894187hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg38456
hg19456
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277095
Samples
Known GenesDEPTOR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561032
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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