A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258219



Internal ID20825259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:55256540..55256879hg38UCSC Ensembl
chr2:55483676..55484015hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6538807
Supporting Variants
Samples
Known GenesMTIF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258219
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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