A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491294



Internal ID21148847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74103501..74131700hg38UCSC Ensembl
chr14:74570204..74598403hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3828200
hg1928200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193771
Samples
Known GenesLIN52
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491294
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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