A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548319



Internal ID20921511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28248432..28253920hg38UCSC Ensembl
chr1:28574943..28580431hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg385489
hg195489
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249652
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548319
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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