A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258588



Internal ID20825628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:208308121..208308777hg38UCSC Ensembl
chr2:209172845..209173501hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38657
hg19657
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545388
Supporting Variants
Samples
Known GenesPIKFYVE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258588
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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