A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491333



Internal ID21148886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24444462..24552454hg38UCSC Ensembl
chr14:24913668..25021660hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38107993
hg19107993
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183746
Samples
Known GenesCMA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491333
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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