A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272321



Internal ID20839361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:121518878..121522505hg38UCSC Ensembl
chr7:121158932..121162559hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg383628
hg193628
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574651
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272321
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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