A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18104833



Internal ID20671873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9706401..9709300hg38UCSC Ensembl
chr3:9748085..9750984hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6366668
Supporting Variants
Samples
Known GenesCPNE9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18104833
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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