A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257546



Internal ID20824586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27331488..27331939hg38UCSC Ensembl
chr2:27554355..27554806hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38452
hg19452
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547569
Supporting Variants
Samples
Known GenesGTF3C2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257546
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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