A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18027641



Internal ID20594681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98770754..98771138hg38UCSC Ensembl
chr15:99313983..99314367hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38385
hg19385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500469
Supporting Variants
Samples
Known GenesIGF1R
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18027641
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00049


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