A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552854



Internal ID20925975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:69433058..69433405hg38UCSC Ensembl
chr2:69660190..69660537hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258892
Samples
Known GenesNFU1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552854
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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