A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541903



Internal ID20915171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:69404278..69404828hg38UCSC Ensembl
chr2:69631410..69631960hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg38551
hg19551
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258291
Samples
Known GenesNFU1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541903
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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