A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552204



Internal ID20925332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:200418537..200419612hg38UCSC Ensembl
chr1:200387665..200388740hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg381076
hg191076
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248252
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552204
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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