A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542465



Internal ID20915724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168543485..168577115hg38UCSC Ensembl
chr1:168512723..168546353hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3833631
hg1933631
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv434n223
Supporting Variantsnssv18248051
Samples
Known GenesXCL1, XCL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542465
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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