A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535681



Internal ID20909035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:232565854..232566420hg38UCSC Ensembl
chr2:233430564..233431130hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257354
Samples
Known GenesEIF4E2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535681
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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