A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553951



Internal ID20927061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:221754497..221755405hg38UCSC Ensembl
chr1:221927839..221928747hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38909
hg19909
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv536n223
Supporting Variantsnssv18249288
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553951
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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