A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549212



Internal ID20922380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:81418482..81419411hg38UCSC Ensembl
chr1:81884167..81885096hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38930
hg19930
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253246
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549212
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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