A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18151239



Internal ID20718279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:102061208..102063642hg38UCSC Ensembl
chr7:101704488..101706922hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg382435
hg192435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6604928
Supporting Variants
Samples
Known GenesCUX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18151239
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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