A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514623



Internal ID20887978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98777001..98799466hg38UCSC Ensembl
chr15:99320230..99342695hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3822466
hg1922466
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182640
Samples
Known GenesIGF1R, MIR4714
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514623
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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