A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554756



Internal ID20927847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:226026720..226027801hg38UCSC Ensembl
chr2:226891436..226892517hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg381082
hg191082
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257174
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554756
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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