A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550903



Internal ID20924045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:70475426..70477433hg38UCSC Ensembl
chr1:70941109..70943116hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg382008
hg192008
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251354
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550903
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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