A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512298



Internal ID20885630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101004154..101513562hg38UCSC Ensembl
chr14:101470491..101979899hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38509409
hg19509409
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187580
Samples
Known GenesMEG9, MIR1185-1, MIR1185-2, MIR1193, MIR1197, MIR134, MIR154, MIR299, MIR300, MIR323A, MIR323B, MIR329-1, MIR329-2, MIR369, MIR376A1, MIR376A2, MIR376B, MIR376C, MIR377, MIR379, MIR380, MIR381, MIR381HG, MIR382, MIR409, MIR410, MIR411, MIR412, MIR485, MIR487A, MIR487B, MIR494, MIR495, MIR496, MIR539, MIR541, MIR543, MIR654, MIR655, MIR656, MIR668, MIR758, MIR889
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512298
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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