A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571708



Internal ID20944779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:42788472..42790278hg38UCSC Ensembl
chr5:42788574..42790380hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg381807
hg191807
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268376
Samples
Known GenesCCDC152
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571708
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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