A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18256183



Internal ID20823223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:176214550..176214920hg38UCSC Ensembl
chr2:177079278..177079648hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38371
hg19371
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545577
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18256183
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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