A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272909



Internal ID20839949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101600965..101604106hg38UCSC Ensembl
chr7:101244245..101247386hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg383142
hg193142
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559971
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272909
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0001


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