A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550055



Internal ID20923207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206199378..206199789hg38UCSC Ensembl
chr2:207064102..207064513hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38412
hg19412
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258524
Samples
Known GenesGPR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550055
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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