A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550883



Internal ID20924025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:37143894..37144658hg38UCSC Ensembl
chr2:37371037..37371801hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg38765
hg19765
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260182
Samples
Known GenesEIF2AK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550883
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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