A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490558



Internal ID21148111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64298630..64380420hg38UCSC Ensembl
chr14:64765348..64847138hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3881791
hg1981791
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194334
Samples
Known GenesESR2, MIR548AZ, TEX21P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490558
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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