A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257214



Internal ID20824254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:227618688..227618828hg38UCSC Ensembl
chr2:228483404..228483544hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6541613
Supporting Variants
Samples
Known GenesC2orf83
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257214
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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