A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495966



Internal ID20869163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69093740..69096802hg38UCSC Ensembl
chr15:69386080..69389142hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg383063
hg193063
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026290
Samples
Known GenesLINC00277, MIR548H4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495966
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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