A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488947



Internal ID21146500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85393961..85503749hg38UCSC Ensembl
chr14:85860305..85970093hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38109789
hg19109789
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184916
Samples
Known GenesLINC00911
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488947
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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