A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18157087



Internal ID20724127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28544228..28548350hg38UCSC Ensembl
chr7:28583846..28587968hg19UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg384123
hg194123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6605845
Supporting Variants
Samples
Known GenesCREB5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18157087
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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