A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549071



Internal ID20922242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:44865233..44865593hg38UCSC Ensembl
chr1:45330905..45331265hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251853
Samples
Known GenesEIF2B3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549071
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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