A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543306



Internal ID20916555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:207800424..207802191hg38UCSC Ensembl
chr2:208665148..208666915hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg381768
hg191768
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258570
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543306
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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