A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538073



Internal ID20911399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:102141053..102146110hg38UCSC Ensembl
chr1:102606609..102611666hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg385058
hg195058
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv285n223
Supporting Variantsnssv18246993
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538073
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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