A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274456



Internal ID20841496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140548804..140549231hg38UCSC Ensembl
chr7:140248604..140249031hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38428
hg19428
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573072
Supporting Variants
Samples
Known GenesDENND2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274456
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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