A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100619



Internal ID20667659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44767668..44786019hg38UCSC Ensembl
chr3:44809160..44827511hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3818352
hg1918352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6361261
Supporting Variants
Samples
Known GenesKIF15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100619
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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