A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539452



Internal ID20912747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:72423719..72426128hg38UCSC Ensembl
chr1:72889402..72891811hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg382410
hg192410
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv235n223
Supporting Variantsnssv18251390
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539452
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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