A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552169



Internal ID20925297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:69007568..69008017hg38UCSC Ensembl
chr1:69473251..69473700hg19UCSC Ensembl
Cytoband1p31.2
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251313
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552169
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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