A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552898



Internal ID20926019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:95714669..96389981hg38UCSC Ensembl
chr1:96180225..96855537hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38675313
hg19675313
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253975
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552898
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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