A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542140



Internal ID20915406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:223786759..223787753hg38UCSC Ensembl
chr1:223974461..223975455hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38995
hg19995
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249333
Samples
Known GenesTP53BP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542140
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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