A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15753656



Internal ID21388997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77616659..77618658hg38UCSC Ensembl
chr15:77909001..77911000hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432260
Supporting Variants
SamplesNB08
Known GenesLINGO1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15753656
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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