A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488960



Internal ID21146513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64314867..64318568hg38UCSC Ensembl
chr14:64781585..64785286hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg383702
hg193702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179036
Samples
Known GenesESR2, MIR548AZ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488960
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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