A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495142



Internal ID21152695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64977472..65017753hg38UCSC Ensembl
chr14:65444190..65484471hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3840282
hg1940282
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196588
Samples
Known GenesCHURC1-FNTB, FNTB, MAX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495142
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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