A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540703



Internal ID20913993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84557829..84558381hg38UCSC Ensembl
chr1:85023512..85024064hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38553
hg19553
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253920
Samples
Known GenesCTBS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540703
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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