A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579875



Internal ID20952946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55379825..55380593hg38UCSC Ensembl
chr15:55672023..55672791hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38769
hg19769
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241050
Samples
Known GenesCCPG1, DYX1C1-CCPG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579875
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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