A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276006



Internal ID20843046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44821745..44821878hg38UCSC Ensembl
chr7:44861344..44861477hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574766
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276006
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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