A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537329



Internal ID20910667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:221754545..221755294hg38UCSC Ensembl
chr1:221927887..221928636hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38750
hg19750
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv536n223
Supporting Variantsnssv18249289
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537329
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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