A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272908



Internal ID20839948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101584484..101585112hg38UCSC Ensembl
chr7:101227764..101228392hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38629
hg19629
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568219
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272908
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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