A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183892



Internal ID20750932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98752480..98786232hg38UCSC Ensembl
chr15:99295709..99329461hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3833753
hg1933753
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513398
Supporting Variants
Samples
Known GenesIGF1R, MIR4714
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183892
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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