A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540027



Internal ID20913319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46053258..46427835hg38UCSC Ensembl
chr3:46094750..46469326hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38374578
hg19374577
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262668
Samples
Known GenesCCR1, CCR2, CCR3, CCR5, CCRL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540027
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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